99-396. Export Certification; Accreditation of Non-Government Facilities  

  • [Federal Register Volume 64, Number 5 (Friday, January 8, 1999)]
    [Rules and Regulations]
    [Pages 1098-1106]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-396]
    
    
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    DEPARTMENT OF AGRICULTURE
    
    Animal and Plant Health Inspection Service
    
    7 CFR Part 353
    
    [Docket No. 95-071-2]
    RIN 0579-AA75
    
    
    Export Certification; Accreditation of Non-Government Facilities
    
    AGENCY: Animal and Plant Health Inspection Service, USDA.
    
    ACTION: Final rule.
    
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    SUMMARY: We are amending the export certification regulations to 
    provide for the establishment of a program under which non-government 
    facilities may become accredited to perform specific laboratory testing 
    or phytosanitary inspection services that may serve as the basis for 
    the issuance of a Federal phytosanitary certificate, export certificate 
    for processed plant products, or phytosanitary certificate for 
    reexport. Prior to this rule, only tests conducted by public 
    laboratories or inspections carried out by Federal, State, or county 
    inspectors or by agents could be used as the basis for the issuance of 
    Federal certificates. The accreditation criteria for particular 
    laboratory testing and phytosanitary inspection services will be 
    developed by the Animal and Plant Health Inspection Service in 
    cooperation with other interested government, industry, academic, or 
    research entities. The accreditation program will provide a mechanism 
    for qualified non-government facilities to become accredited to perform 
    testing or inspection services that may be used as supporting 
    documentation for the issuance of certificates for certain plants or 
    plant products.
    
    EFFECTIVE DATE: February 8, 1999.
    
    FOR FURTHER INFORMATION CONTACT: Mr. Narcy G. Klag, Accreditation 
    Program Manager, Phytosanitary Issues Management, PPQ, APHIS, 4700 
    River Road Unit 140, Riverdale, MD 20737-1236; (301) 734-8469.
    
    SUPPLEMENTARY INFORMATION:
    
    Background
    
        The export certification regulations in 7 CFR part 353 (referred to 
    below as the regulations) set forth the procedures for obtaining 
    certification for plants and plant products offered for export or 
    reexport. Under the regulations, tests conducted by public laboratories 
    or inspections carried out by Federal, State, or county inspectors or 
    by agents may be used as the basis for the issuance of Federal 
    certificates. Export certification is not required by the regulations; 
    rather, it is provided by the Animal and Plant Health Inspection 
    Service (APHIS) as a service to exporters who are shipping plants or 
    plant products to countries that require phytosanitary certification as 
    a condition of entry. After assessing the condition of the plants or 
    plant products intended for export, relative to the receiving country's 
    regulations, an inspector will issue an internationally recognized 
    phytosanitary certificate (PPQ Form 577), a phytosanitary certificate 
    for reexport (PPQ Form 579), or an export certificate for processed 
    plant products (PPQ Form 578), if warranted. The regulations also 
    provide for an industry-based certification, under certain conditions, 
    of certain low-risk plant products such as kiln-dried lumber offered 
    for export.
        On November 25, 1997, we published in the Federal Register (62 FR 
    62699-62707, Docket No. 95-071-1) a proposal to amend the regulations 
    to provide for the establishment of a program under which non-
    government facilities could become accredited to perform specific 
    laboratory testing or phytosanitary inspection services that could 
    serve as the basis for the issuance of a Federal phytosanitary 
    certificate, export certificate for processed plant products, or 
    phytosanitary certificate for reexport.
        We solicited comments concerning our proposed rule for 60 days 
    ending January 26, 1998. We received 34 comments by that date. The 
    comments were from processors and distributors of agricultural 
    commodities, State and county agricultural agencies, a seed trade 
    association, seed companies, crop improvement associations, a 
    university laboratory, private testing and certification services, an 
    association of State agricultural officials, laboratory accreditation 
    organizations, a foreign plant health agency, and an association of 
    seed certifying officials. Although all of the commenters supported the 
    concept of an accreditation program, all but six of them had specific 
    concerns, questions, or suggestions regarding the proposed 
    accreditation program. The comments are addressed below.
    
    [[Page 1099]]
    
    Role of Accredited Facilities
    
        Several commenters referred to accredited facilities as ``private 
    certifiers'' or as having responsibility for the issuance of 
    phytosanitary certificates. We wish to make it clear that accredited 
    facilities will not be ``certifiers,'' nor will accredited facilities 
    issue phytosanitary certificates. Rather, an accredited facility would 
    perform specific tests or inspections that would serve as the basis for 
    phytosanitary certification; phytosanitary certificates will continue 
    to be issued by Federal, State, or county-level inspectors, as provided 
    by the regulations.
    
    Handling of Samples
    
        Two commenters raised the issue of the handling of samples 
    submitted for testing or inspection. The commenters were concerned that 
    the proposed rule did not address issues such as who would collect and 
    prepare samples for testing or inspection and how the integrity of 
    samples would be maintained during movement and while at the accredited 
    facility. One of the commenters stated that APHIS should specify how 
    all samples are to be collected and handled, while the second commenter 
    suggested that a sample handling accreditation program be made part of 
    the regulations.
        We agree with the commenters that the proper handling of samples is 
    important to any laboratory testing or inspection program. Because the 
    procedures and requirements for the collection and handling of samples 
    will likely vary to some extent from plant to plant or product to 
    product, we believe that sample collection and handling should be 
    addressed in each set of specific accreditation standards as they are 
    prepared, rather than in a general way in the regulations. Further, 
    because the sample handling requirements will be part of each set of 
    specific accreditation standards, we do not believe that it is 
    necessary to establish a separate sample handling accreditation 
    program.
    
    Conflict of Interest
    
        Two commenters suggested that APHIS or State agencies should act as 
    an intermediary between accredited laboratories and their customers, 
    serving as the conduit for contracting and payment for services and the 
    submission of samples for testing. Two other commenters stated that 
    APHIS must ensure that laboratory analyses are not performed by anyone 
    having an interest in the product to avoid conflicts of interest. These 
    four commenters sought to separate the entity performing an inspection 
    or test from the entity for whom the work is performed in order to 
    prevent any influence or bias. One of them noted that the current 
    regulations in Sec. 353.6(a)(3) prohibit agents from performing 
    inspections of any plants or plant products in which they or a family 
    member are directly or indirectly financially interested, and stated 
    that the same conflict of interest rules should apply to accredited 
    facilities. Two different commenters foresaw the possibility that an 
    accredited facility might be a division or affiliate of a company that 
    would use its testing or inspection services and asked how APHIS would 
    deal with the potential conflicts of interest inherent in a facility 
    testing or inspecting its own plants or plant products.
        The issue in all of the comments summarized in the previous 
    paragraph appears to be whether or not an accredited facility that is 
    connected in some way to a commercial entity for which it is performing 
    a service will be able to conduct unbiased tests or inspections and 
    accurately report the results of those tests or inspections. The 
    commenters appear to be worried that an accredited facility might 
    tailor test protocols or alter results in order to get the ``right'' 
    answer that will please the commercial entity with which the facility 
    is associated.
        We acknowledge that it is possible that an accredited facility 
    could attempt to provide inaccurate information to an inspector in 
    order to secure a phytosanitary certificate. However, given the 
    investment of time, money, and other resources that becoming accredited 
    would require, we do not believe that an accredited facility would risk 
    having its accreditation withdrawn by falsely certifying that a 
    specific test or inspection had been conducted and its results 
    faithfully reported.
        Falsified test or inspection results can be detected by inspectors 
    conducting post-accreditation reviews or audits of facilities or 
    through random checks by certifying officials of plants or plant 
    products for which a phytosanitary certificate is sought. Under 
    Sec. 353.8(b)(4), facilities must agree to be periodically assessed and 
    evaluated by means of proficiency testing or check samples in order to 
    retain accreditation. Further, the tests or inspections that accredited 
    facilities will perform are for pests or diseases that are likely to 
    manifest themselves at some point. Presumably, an importing country is 
    asking for a phytosanitary certificate because a certain pest or 
    disease that may be present in the United States does not exist or is 
    not widely prevalent in that importing country; if the pest or disease 
    is detected in the importing country following the receipt of a 
    shipment certified on the basis of falsified test results, it is likely 
    that the pest or disease will be traced to that shipment. If it can be 
    confirmed that the exporting company, through its accredited facility, 
    used false test results to obtain a phytosanitary certificate, several 
    consequences are possible: The facility's accreditation could be 
    withdrawn, the facility or its parent company could be subject to civil 
    or even criminal penalties in the United States or the importing 
    country, and the parent company would likely lose the trust--and the 
    business--of its customers. We believe that the likelihood of detection 
    and the consequences associated with falsifying results will serve as a 
    deterrent in those cases where such deterrence is necessary.
    
    Composition of Assessment Teams
    
        One commenter asked if competitors of a facility seeking 
    accreditation would be involved in a facility's pre-accreditation 
    assessment. The commenter stated that such participation would be 
    inappropriate because the assessment team members must be completely 
    impartial and assess the facility on the standards established by the 
    rule without any appearance of bias. Another commenter asked if State 
    plant regulatory agencies would be involved in the pre-accreditation 
    assessment process and post-accreditation activities.
        We do not anticipate that we will seek the participation of 
    operators or employees of commercial laboratories or inspection 
    services in the pre-accreditation assessment process. We do expect that 
    there will be instances when we will seek the formal assistance of our 
    cooperators in State plant regulatory agencies in the pre-accreditation 
    assessment process or in post-accreditation facility visits and 
    reviews. In addition, we would welcome the participation of our State 
    cooperators in any accreditation activities being conducted in their 
    respective States.
    
    Post-Accreditation Supervision
    
        One commenter stated that his organization could support the 
    concept of accreditation only if APHIS maintained continuous, day-to-
    day oversight of the program through the appointment of an 
    accreditation manager who would administer the application procedures 
    and audits, arrange for proficiency testing, develop and provide 
    training for seed health tests and field inspection procedures, issue 
    accreditation credentials, maintain accreditation records, and 
    establish
    
    [[Page 1100]]
    
    standard tests for laboratory and field inspection procedures.
        The need for program management such as that described by the 
    commenter was recognized by APHIS at the time the proposed rule was 
    being prepared, so there are already plans to appoint an accreditation 
    manager within APHIS' Plant Protection and Quarantine program to 
    perform the tasks identified by the commenter.
        Another commenter questioned whether APHIS had sufficient staff to 
    implement and adequately monitor the accreditation program. The 
    commenter stated that there are universities and State departments of 
    agriculture that could serve as accreditors to more efficiently perform 
    the actual accreditation work for APHIS; APHIS' role could be purely 
    administrative, with the bulk of operational work being accomplished by 
    the State-level accreditors.
        As noted above, an accreditation manager will be appointed in APHIS 
    to oversee the program's operation. We anticipate that the 
    accreditation manager will work closely with the export certification 
    program's traditional cooperators at the State and county level, 
    relying on them for advice and assistance with regard to accreditation 
    activities in their geographic area or within their realm of expertise. 
    As with other aspects of the program, the extent to which State 
    cooperators will become involved in accreditation-related activities 
    will depend largely on demand for accreditation and the number of 
    facilities that become accredited.
        One commenter had several questions regarding post-accreditation 
    supervision of facilities: What will be the frequency of post-
    accreditation audits or inspections? Will State plant regulatory 
    agencies be able to request an audit or inspection if an irregularity 
    is noted or a complaint is received? Will State plant regulatory 
    agencies be notified of the results of those audits or inspections?
        The frequency of post-accreditation audits and inspections will be 
    determined, at least in part, by the type of service a facility becomes 
    accredited to perform. The performance of field inspections and even 
    some types of laboratory testing will be subject to seasonal changes 
    and other variables, so it would be difficult to prescribe a universal 
    audit schedule as part of this final rule. Thus, the frequency of post-
    accreditation audits and inspections for a particular area of 
    accreditation will be determined at the same time the specific 
    standards for accreditation in that area are developed.
        We would encourage State plant regulatory agencies, as well as 
    other entities that have dealings with an accredited facility, to 
    report any observed deficiencies or irregularities in an accredited 
    facility to the APHIS accreditation manager or to an inspector. APHIS 
    will review all reports received and, as appropriate, will perform an 
    inspection or audit in order to resolve any issues that arise regarding 
    accredited facilities. As cooperators in APHIS' phytosanitary export 
    certification program, State plant regulatory agencies will be kept 
    informed of developments in the program, including those related to 
    accredited facilities.
        One other commenter was concerned that the quality of inspection 
    could suffer under an accreditation plan. Although he offered no 
    specific examples, the commenter stated that in some situations where 
    self-inspection has been performed, quality problems such as 
    overlooking specific infestations or diseases have manifested 
    themselves. If the quality of inspection is reduced or is unacceptable 
    to an importing country, the commenter concluded, the U.S. 
    phytosanitary inspection system as a whole may come under scrutiny.
        We agree with the commenter's assertion that the quality of 
    inspection must be maintained to ensure the continued confidence of our 
    trading partners. We believe that the accreditation program provided 
    for by this final rule, with its focus on standards and required levels 
    of performance, will preserve--and even enhance--the quality and 
    credibility of the U.S. phytosanitary certification program.
    
    Issuance of Certificates
    
        One commenter asked if accredited facilities would apply to APHIS 
    or to State cooperators for export certificates and, if application for 
    a certificate was made to a State cooperator, whether the State 
    cooperator would be required to issue a certificate.
        The regulations in Sec. 353.7 state that phytosanitary certificates 
    are signed and issued by inspectors; an inspector, as defined in 
    Sec. 353.1, could be either an APHIS employee or a State or county 
    plant regulatory official designated by the Secretary of Agriculture to 
    inspect and certify to shippers and other interested parties as to the 
    phytosanitary condition of plant products. Any shipment offered for 
    certification that meets the requirements of the importing country and 
    is in compliance with the regulations is expected to be certified; to 
    do otherwise would be a disservice to--and likely challenged by--those 
    individuals seeking a certificate.
        On a similar note, a commenter from a county agricultural agency 
    stated that she was concerned about the possibility of placing the 
    county in a position of greater liability if she had to issue a 
    phytosanitary certificate based on laboratory analysis or field 
    inspections completed by a private company rather than a public agency.
        No liability should attach to a certifying official as long as the 
    certification is made in accordance with the regulations. The 
    certifying statement on the phytosanitary certificate states that 
    ``This is to certify that the plants or plant products described below 
    have been inspected according to appropriate procedures and are 
    considered free from quarantine pests * * *'' Using test or inspection 
    results provided by an accredited facility is an appropriate and 
    defensible procedure.
    
    Costs of Accreditation
    
        Several commenters were opposed to the provisions of the proposed 
    rule that would require the operator of a facility seeking 
    accreditation to enter into a trust fund agreement with APHIS prior to 
    accreditation. Several commenters stated that private entities need to 
    know in advance what the costs associated with the accreditation 
    process will be in order to be able to accurately calculate all costs 
    and benefits of the system. The commenters further stated that the 
    failure to accurately calculate all costs of accreditation, at all 
    levels of administration, could lead to an accreditation system that is 
    not viable, cost effective, or competitive in delivering phytosanitary 
    certification services. The commenters suggested that the trust fund 
    requirement apply only to entities that have not completed the 
    necessary cost analyses for implementing an accreditation scheme for 
    their constituents, or for entities that have not established a cash 
    reserve to cover the startup and long-term administration costs of 
    accreditation.
        Given the tenor of those comments, it appears that the purpose and 
    scope of the trust fund agreement may not have been fully explained in 
    the proposed rule. We do not intend for the trust fund to be a single 
    pool of money funded by a particular industry segment from which APHIS 
    will draw to fund its activities in a certain area of accreditation. 
    Associations representing certain industry sectors may certainly play a 
    role in helping to develop accreditation standards that will be applied 
    to facilities within their industry, but when it comes to the actual 
    accreditation of facilities, those
    
    [[Page 1101]]
    
    facilities will individually enter into trust fund agreements with 
    APHIS to cover the costs of their accreditation.
        Under a trust fund agreement, APHIS will, in advance, provide the 
    facility's operator with an estimate of the costs it expects to incur 
    through its involvement in the pre-accreditation assessment process. As 
    particular standards are developed, we will be better able to forecast 
    that cost and the costs of the maintenance of the facility's 
    accreditation. The operator of the facility would then deposit a 
    certified or cashier's check with APHIS for the amount of the estimated 
    costs, and the pre-accreditation assessment process would begin. If the 
    deposit is not sufficient to meet all costs incurred by APHIS, the 
    facility operator, under the terms of the trust fund agreement, would 
    deposit another certified or cashier's check with APHIS for the amount 
    of the remaining costs before APHIS' services would be completed. After 
    a final audit at the conclusion of the pre-accreditation assessment, 
    any overpayment of funds would be returned to the operator of the 
    facility or held on account until needed for future activities related 
    to the maintenance of the facility's accreditation.
        Because this is a new program, we cannot say with certainty what 
    all the costs will be and whether this trust fund agreement process 
    will be the best way of handling the recovery of the costs of our 
    participation in the accreditation process. Trust fund agreements have 
    been used successfully in other APHIS programs, and we believe that 
    they will be useful in this accreditation program. However, if the 
    agreement process proves unwieldy or unworkable, we will propose to 
    amend the regulations to modify the way in which APHIS recovers its 
    costs.
    
    Costs of Services
    
        One commenter was concerned that APHIS' intention to recover all 
    costs associated with its administration of the accreditation program 
    would result in fees that would be so high that they would render the 
    program infeasible.
        As explained in the proposed rule, the administrative expenses that 
    we expect to incur and recover will be for items such as laboratory 
    fees for evaluating check test results and all salaries, travel 
    expenses, and other incidental expenses incurred by APHIS in performing 
    the pre-accreditation assessment. As long as we could determine that it 
    would be feasible and practical to establish an accreditation program 
    in a particular area to begin with, we do not expect that costs related 
    to those activities would be prohibitive. To make that consideration 
    clear, we have amended Sec. 353.8(b)(1) in this final rule to provide 
    that APHIS will make a determination regarding the practicality of 
    establishing an accreditation program in a particular area before 
    beginning the process of developing the standards that would be 
    applicable to accreditation in that area. Further, participation in the 
    accreditation program will be voluntary, and an estimate of costs will 
    be provided to each applicant before APHIS begins any accreditation-
    related activities, so there will be ample opportunity for the 
    applicant to consider whether accreditation will be desirable from a 
    cost perspective.
        One commenter stated that the services of accredited facilities 
    could become very expensive for industry if private entities providing 
    services charged enough to cover their expenses. The commenter 
    concluded that because some State agencies charge less than what is 
    actually necessary to cover their expenses, the fees charged by private 
    facilities will likely exceed the fees charged by government 
    facilities. Although it is possible that an accredited entity could 
    charge a higher fee than a public agency, a customer may still choose 
    to use the accredited entity's services if the customer receives an 
    added benefit such as faster reporting of results. However, if an 
    accredited entity charges fees that are perceived to be too high by 
    prospective customers, it is likely that those customers would take 
    their business elsewhere, i.e., to a government facility or other 
    accredited facility. Private entities providing inspection or testing 
    services will be subject to the same market forces as any other entity 
    providing services and will have to maintain a competitive fee schedule 
    to remain in business.
    
    Standards for Field Inspection
    
        One commenter agreed that the four major accreditation assessment 
    areas (physical plant, equipment, methods of testing or inspection, and 
    personnel) were appropriate, but stated that quality control is more 
    problematic regarding the accreditation of field inspectors. The 
    commenter noted that an accreditor cannot place a diseased or infested 
    plant in a field as part of a pre-accreditation assessment to see if it 
    is detected and reported. The commenter concluded by stating that 
    special attention must be given to the need for credible assessment 
    mechanisms when standards are set for accrediting private entities to 
    perform field inspections.
        We acknowledge that assessing proficiency in the area of field 
    inspection may prove to be more of a challenge than assessing 
    proficiency in the somewhat more easily quantifiable area of laboratory 
    testing. The development of specific standards for accreditation to 
    conduct field inspections (as well as all other specific standards) 
    will be a collaborative process, as APHIS will seek the input, 
    cooperation, and comments of industry, academic, government, or other 
    personnel with expertise or interest in the areas that will be 
    assessed. We are confident that this collaborative process will result 
    in field inspection accreditation standards that will provide an 
    accurate assessment of an individual or entity seeking accreditation in 
    that area.
    
    Withdrawal or Denial of Accreditation
    
        One commenter was concerned that the 10 days that would be provided 
    for the operator of a facility to appeal a denial or withdrawal of 
    accreditation would not allow enough time to develop an adequate 
    appeal. The commenter stated that 30 days should be provided to file an 
    appeal, and that the Administrator's decision regarding an appeal 
    should also be made within 30 days, rather than the proposed ``as 
    promptly as circumstances permit.''
        We do not believe that it is necessary to extend the time for a 
    person to submit an appeal. To appeal a denial, the operator must 
    provide the reasons why he or she believes that accreditation was 
    wrongfully denied; to appeal a withdrawal, the operator must provide 
    all of the facts and reasons upon which he or she relies to show that 
    the reasons for the proposed withdrawal are incorrect or do not support 
    the withdrawal. Because APHIS will inform the operator of all of the 
    reasons on which it based its denial or withdrawal of accreditation, 
    and the appeal is, in essence, the operator's specific response to each 
    of those stated reasons, we believe that 10 days is a sufficient amount 
    of time for an operator to prepare an appeal. Although the 
    Administrator will, in most cases, be able to respond to an appeal in 
    less than the 30-day limit suggested by the commenter, we have retained 
    ``as promptly as circumstances permit'' as the time frame for the 
    Administrator's decision so as not to limit our ability to investigate 
    or review the circumstances surrounding a withdrawal or denial in light 
    of the information provided in the appeal.
        Two other commenters were concerned about the length of time that 
    could potentially pass before the withdrawal of a facility's 
    accreditation became effective due to the proposed provisions for the 
    operator to appeal the withdrawal. Both commenters stated
    
    [[Page 1102]]
    
    that allowing an accredited entity to continue to perform phytosanitary 
    work while an appeal was filed and heard could result in the issuance 
    of additional invalid phytosanitary certificates. One of those 
    commenters further stated that the proposed provision for immediate 
    withdrawal to protect ``public health, interest, or safety'' 
    constituted a high legal standard that might be easily and often 
    challenged.
        As noted by one of the commenters, the regulations will provide for 
    the withdrawal of a facility's accreditation to become effective 
    immediately when the Administrator determines that an immediate 
    withdrawal action is necessary to protect the public health, interest, 
    or safety. The withdrawal will be effective upon oral or written 
    notification, whichever is earlier, to the operator of the facility and 
    will continue in effect pending the completion of the proceeding, and 
    any judicial review of the proceeding, unless otherwise ordered by the 
    Administrator. Because a credible phytosanitary export certification 
    program, which greatly facilitates U.S. export trade in plants and 
    plant products, is clearly in the public interest, we believe that we 
    can justify the immediate withdrawal of a facility's accreditation when 
    circumstances warrant.
    
    Accreditation of Government Facilities
    
        Several commenters discussed the apparent disparity between the 
    requirements for government and non-government facilities, each making 
    an argument for a different degree of uniformity between the public and 
    private facilities. One commenter stated that APHIS should provide 
    government facilities with copies of the standards and procedures and 
    minimum recordkeeping guidelines, and should provide training in the 
    standards at no charge to the government facility as part of the 
    cooperative agreement between APHIS and the States. A second commenter 
    stated that APHIS should require all entities, both government and non-
    government, to conduct their diagnostic tests or field inspections in 
    accordance with the standards and procedures. A third commenter 
    suggested that government facilities should be able to become 
    accredited if they choose to do so, while a fourth commenter stated 
    that accreditation should be required for both government and non-
    government facilities. Another commenter stated that the draft North 
    American Plant Protection Organization (NAPPO) accreditation standards 
    mentioned in the proposed rule clearly state that all personnel 
    carrying out the same phytosanitary certification inspection functions, 
    be they government or non-government personnel, must meet the same 
    standards, so government facilities should be required to be 
    accredited. All of these commenters cited the need for standard testing 
    and inspection protocols and warned that failure to provide for 
    coordination in that area could result in discrepancies in the U.S. 
    phytosanitary certification system and a subsequent erosion in the 
    confidence of importing countries with regard to that system.
        The accreditation provided for by the final rule is, in essence, 
    the means by which APHIS can approve a non-government facility to 
    perform, in an official capacity, the same tests or inspections that 
    Federal and State laboratories and personnel currently perform in 
    support of the phytosanitary export certification program. As such, 
    there is no reason to require facilities operated by a State or other 
    governmental entity to become accredited. That being said, we do agree 
    with those commenters who have pointed out the need for standardization 
    and uniformity in phytosanitary testing and inspection. When developing 
    specific standards for a particular area of accreditation, we will 
    solicit and encourage the participation of all interested parties in 
    the public and private sectors and academia, and we expect the 
    resulting standards will reflect the best available science, processes, 
    and methods. Once completed, those standards will be used not only to 
    evaluate facilities seeking accreditation, but will be distributed to 
    Federal and State facilities performing phytosanitary certification 
    work to ensure that they are using the best available science, 
    processes, and methods.
    
    Promulgation of Standards
    
        Several commenters were concerned that the specific standards for 
    accreditation would be subject to notice and comment rulemaking after 
    they had been developed and before they could be applied to the 
    accreditation of non-government facilities. These commenters stated 
    that having to publish standards in the Federal Register would result 
    in delays that would have a negative effect on the entire accreditation 
    program. Most of these commenters stated that APHIS must make a clear 
    distinction between those standards that would require publication in 
    the Federal Register and those that would not, suggesting that basic, 
    generally applicable standards might be promulgated through rulemaking, 
    while items with more limited applicability, such as the protocols for 
    a specific test, could be made available as part of the guidelines that 
    apply to a specific area of accreditation.
        We recognize the commenters' concerns and agree that the 
    development and promulgation of specific standards must be accomplished 
    in a manner that will allow the program to grow and adapt to new 
    technologies without undue process-driven delays. At the same time, 
    however, we must balance that desire for responsiveness and flexibility 
    with the need for program standards that are enforceable and that have 
    been developed with the necessary level of public participation. 
    Because this final rule only makes specific accreditation programs 
    possible and does not itself contain any specific standards, it is 
    difficult to conclusively define what will and will not be included 
    when standards are published. As an example, an accreditation standard 
    might call for a particular test to be performed; while the type and 
    purpose of the test will be published with the criteria for 
    interpreting test results and other aspects of the standard, the 
    detailed instructions and protocols for conducting the actual test 
    itself would not necessarily have to be published. Our goal is to 
    develop and promulgate standards in a manner that will allow the 
    process to be responsive and flexible while ensuring that the standards 
    themselves are fair and enforceable.
    
    Use of Subcontractors
    
        Four of the commenters were concerned about the provisions of the 
    proposed rule that would allow the use of subcontractors by accredited 
    facilities. One comment, from a foreign agricultural agency, stated 
    that his agency viewed the use of subcontractors as a further 
    delegation by APHIS of its phytosanitary certification duties. The 
    commenter closed by saying that APHIS must negotiate such delegations 
    with its foreign counterparts before proceeding with allowing the use 
    of contractors. The second commenter noted that although the proposed 
    rule would provide for a review of a subcontractor's qualifications, 
    there are no limits placed on the services the subcontractor could 
    provide. The commenter was concerned that an accredited facility might 
    use a subcontractor to, for example, entirely conduct a test that the 
    facility had been accredited to conduct. The commenter also pointed out 
    that the proposed rule did not prohibit a subcontractor to itself use a 
    subcontractor. The third commenter was concerned that an
    
    [[Page 1103]]
    
    accredited facility that was facing the withdrawal of its accreditation 
    might attempt to shift the blame for their shortcomings to a 
    subcontractor and simply fire one subcontractor and hire another in an 
    effort to retain accreditation. The fourth commenter stated that 
    allowing the use of subcontractors by accredited facilities would make 
    it very difficult to maintain program credibility and would allow for 
    too much extended liability.
        We believe that all four of the commenters have made valid points 
    that bring into question the advisability of allowing accredited 
    facilities to use subcontractors. Therefore, in this final rule, we 
    have eliminated the reference to the use of subcontractors that had 
    been in Sec. 353.8(b)(3)(iv) of the proposed rule.
    
    Use of International Standards
    
        Two of the commenters recommended that APHIS utilize private sector 
    accreditation services for government and non-government laboratories. 
    These commenters stated that accrediting laboratories in accordance 
    with the International Standards Organization's (ISO's) internationally 
    recognized ISO Guide 25 would be a more reasonable and less burdensome 
    approach to accreditation and would be more easily recognized 
    internationally. One commenter noted that other Federal agencies accept 
    third-party laboratory accreditation in areas such as environmental 
    lead and asbestos or electromagnetic compatibility testing. 
    Additionally, that commenter stated, Public Law 104-113 mandates the 
    utilization of private sector laboratory accreditation services.
        As explained above in the response to a previous comment, the 
    accreditation program provided by this final rule is a way for APHIS to 
    approve a non-government facility to perform tests or inspections in 
    support of the phytosanitary export certification program. The program 
    is not intended as, nor has it been presented as, a full-blown 
    laboratory evaluation and accreditation program such as those provided 
    under the auspices of the ISO. The underlying principles of ISO 
    certification, such as quality documentation and accountability, 
    certainly will be applied when specific standards are developed, but we 
    do not believe that it is necessary for a non-government facility to 
    receive ISO 25 certification before it can perform testing or 
    inspection services under the phytosanitary export certification 
    program.
    
    Qualifications
    
        One commenter asked what the minimum qualifications for the 
    accreditation of these private phytosanitary services would be, and how 
    and when the standards would be established. Two other commenters 
    stated that the minimum qualifications for accredited inspectors must 
    be established and should be at least equal to the minimum 
    qualifications required of county, State, or Federal inspectors.
        Specific qualifications for personnel involved in any particular 
    area of accreditation are not within the scope of this final rule. As 
    discussed in the proposed rule, personnel standards are one of the 
    areas in which non-government facilities will be assessed and will, 
    therefore, be one of the areas for which specific standards will be 
    developed. Generally speaking, the qualifications of employees of non-
    government facilities will be similar to those of government laboratory 
    personnel and inspectors. The draft NAPPO standard for accreditation 
    mentioned in the proposed rule states that accredited personnel should 
    not be held to standards that are higher than those for government 
    personnel, a concept with which we agree.
    
    Availability of Information
    
        Two of the commenters wanted to know if the information generated 
    by accredited facilities in the course of their inspection or testing 
    activities would be available for review by APHIS or its State 
    cooperators. One of the commenters stated such data must be available 
    for review to ensure the validity of the testing process. The other 
    commenter stated that because State plant regulatory agencies are 
    cooperators with APHIS in both pest detection and export commodity 
    certification, it is essential that States have access to such 
    information in order to maintain the credibility of their own 
    activities in those areas.
        As standards are developed for specific areas of accreditation, we 
    will ensure that recordkeeping is addressed in a manner appropriate to 
    each area of accreditation. In general, we expect to require that 
    records related to a facility's area of accreditation be made available 
    to APHIS during the pre-accreditation assessment and during subsequent 
    post-accreditation reviews or audits. Similarly, the specific standards 
    will include, as appropriate, provisions for each accredited facility 
    to report pests and diseases to APHIS or the State plant health agency 
    for further action.
    
    Notification of Changes
    
        Two commenters noted that the proposed regulations call for a 
    facility to notify APHIS ``as soon as circumstances permit'' when there 
    is a change in key management personnel or facility staff, or when 
    there is a change involving the location, ownership, physical plant, 
    equipment, or relevant conditions at the plant. Both commenters stated 
    that ``as soon as circumstances permit'' was too vague a time frame 
    given the potential importance of such changes. One of those commenters 
    suggested that a facility should be required to notify APHIS within 48 
    hours of such changes, while the other recommended that notice be given 
    to APHIS within 10 days. We agree with the commenters that a more 
    concrete time frame for notification is desirable given the potential 
    impact of such changes, so we have amended paragraphs (b)(4)(v) and 
    (b)(4)(vi) of Sec. 353.8 to require the operator of a facility to 
    notify APHIS as soon as possible, but no more than 10 days following 
    its occurrence, of any change in the elements set forth in those 
    paragraphs.
        Therefore, based on the rationale set forth in the proposed rule 
    and in this document, we are adopting the provisions of the proposal as 
    a final rule with the changes discussed in this document.
    
    Executive Order 12866 and Regulatory Flexibility Act
    
        This rule has been reviewed under Executive Order 12866. The rule 
    has been determined to be significant for the purposes of Executive 
    Order 12866 and, therefore, has been reviewed by the Office of 
    Management and Budget.
        This rule amends the export certification regulations to provide 
    for the establishment of a program under which non-government 
    facilities may become accredited to perform specific laboratory testing 
    or phytosanitary inspection services that could serve as the basis for 
    the issuance of Federal phytosanitary certificates, phytosanitary 
    certificates for reexport, or export certificates for processed plant 
    products. The accreditation criteria for particular laboratory testing 
    and phytosanitary inspection services will be developed by APHIS in 
    cooperation with other interested individuals or government, industry, 
    academic, or research entities. As specific accreditation criteria are 
    developed, the accreditation program will provide a mechanism for 
    qualified non-government facilities to become accredited to perform 
    testing or inspection services that may be used as supporting 
    documentation for the
    
    [[Page 1104]]
    
    issuance of certificates for certain plants or plant products.
        The regulations in this rule are intended only to provide a 
    framework upon which accreditation programs for specific functions may 
    be established, so they will not, in and of themselves, entail any 
    costs to APHIS or any non-government facility. However, any specific 
    accreditation program that is established under these regulations will 
    entail costs to both the entities being accredited and the accrediting 
    body, i.e., APHIS. Because the accreditation program is expected to be 
    self-supporting, the costs to APHIS will be recouped through 
    accreditation fees. The fees charged by APHIS in connection with the 
    initial accreditation of a non-government facility and the maintenance 
    of that accreditation will, therefore, have to be adequate to recover 
    the costs incurred by the government in the course of APHIS' 
    accreditation activities. We expect that the costs that will be 
    reimbursed will be largely attributable to the cost of transportation 
    for the assessors to travel to the site of the facility, lodging for 
    the assessors, their salary and per diem, any laboratory fees charged 
    for evaluating check test results, and administrative expenses. Costs 
    for specific accreditation programs will vary depending on the range of 
    activities for which a facility seeks accreditation, the number of 
    assessors needed to adequately conduct a pre-accreditation assessment, 
    the type and number of any proficiency tests that will have to be 
    conducted, and the frequency with which post-accreditation evaluation 
    activities such as check tests and site visits will have to be 
    conducted.
        The regulations stipulate that APHIS will provide an estimate of 
    its anticipated fees to the operator of the facility prior to 
    undertaking any activities that will result in fees being charged to a 
    facility. Participation in any accreditation program developed under 
    these regulations will be voluntary. At this time, we estimate that 15 
    individual non-government facilities are likely to seek and maintain 
    accreditation annually on about 82 accredited procedures, as long as 
    the costs of participating in an accreditation program are lower than 
    the benefits they receive from the program. As a result, this program 
    will have to meet the test of the marketplace.
        The domestic seed industry, through the American Seed Trade 
    Association, has indicated its interest in establishing an 
    accreditation program for seed health testing and field inspection of 
    seed, so we have used the domestic seed industry to illustrate the 
    potential benefits that may result from the establishment of specific 
    accreditation programs.
        The seed industry is expected to benefit from the establishment of 
    an accreditation program because domestic seed exporters routinely 
    require the services of inspectors and agents in order to obtain the 
    phytosanitary certification required by most, if not all, importing 
    countries; benefits can be realized in terms of more timely 
    certifications, which in turn can lead to reduced costs as well as 
    increased U.S. exports.
        The value of seed exported from the United States to other 
    countries continues to grow rapidly, from $665 million in 1994-95 (July 
    to June), to $705 million in 1995-96, to more than $800 million 
    projected for 1996-97. There has been a concomitant rise in demand for 
    laboratory testing and phytosanitary inspection services to meet other 
    countries' import requirements. The ability of Federal, State, and 
    county testing and inspection services to meet this growing demand will 
    be increasingly strained. Already there are instances in which the 
    accreditation of non-government facilities would have prevented the 
    loss of export sales.
        For example, some seed export opportunities have been forfeited 
    because the results of pre-harvest field inspections are usually not 
    known until after harvest. It is common for seed from several fields to 
    be blended before shipment. If the sample from one field is 
    subsequently reported to contain an actionable pest, then none of the 
    blended seed--which may have been harvested from as many as eight or 
    nine fields--could be exported. In one case in which this occurred, the 
    affected seed company lost foreign sales worth $250,000. Such losses 
    are much less likely to occur if there is more timely reporting of pre-
    harvest inspections; accredited non-government inspection facilities 
    may be able to make such timely reports. In general, non-government 
    testing and inspection services are expected to be completed with 
    minimal delay, leading to greater marketing flexibility and lower risk 
    of lost sales.
        Additional benefits, of even greater potential significance, can be 
    gained through the standardization of testing and inspection protocols 
    that will result from the establishment of accreditation standards, 
    particularly when internationally recognized standards are used. Major 
    seed trading partners of the United States, such as Canada, France, and 
    The Netherlands, have national seed health organizations that address 
    seed health issues in part by employing laboratory accreditation 
    protocols. The standards that will underlie the accreditation of non-
    government facilities in the United States can help reduce the 
    differences among international phytosanitary regulations, thereby 
    expediting U.S. seed exports.
        Accreditation of non-government facilities, by promoting more 
    streamlined exports based on internationally recognized standards, can 
    also be expected to benefit exports outside of the seed industry. As a 
    self-supporting system, private firms that expect benefits in excess of 
    costs of accreditation are likely to participate. In addition to the 
    net benefits received by these firms directly, society as a whole will 
    benefit from enhanced trade.
        Under these circumstances, the Administrator of the Animal and 
    Plant Health Inspection Service has determined that this action will 
    not have a significant economic impact on a substantial number of small 
    entities.
    
    Executive Order 12372
    
        This program/activity is listed in the Catalog of Federal Domestic 
    Assistance under No. 10.025 and is subject to Executive Order 12372, 
    which requires intergovernmental consultation with State and local 
    officials. (See 7 CFR part 3015, subpart V.)
    
    Executive Order 12988
    
        This rule has been reviewed under Executive Order 12988, Civil 
    Justice Reform. This rule: (1) Preempts all State and local laws and 
    regulations that are inconsistent with this rule; (2) has no 
    retroactive effect; and (3) does not require administrative proceedings 
    before parties may file suit in court challenging this rule.
    
    Paperwork Reduction Act
    
        In accordance with the Paperwork Reduction Act of 1995 (44 U.S.C. 
    3501 et seq.), the information collection or recordkeeping requirements 
    included in this rule have been approved by the Office of Management 
    and Budget (OMB) under OMB control number 0579-0130.
    
    Regulatory Reform
    
        This action is part of the President's Regulatory Reform 
    Initiative, which, among other things, directs agencies to remove 
    obsolete and unnecessary regulations and to find less burdensome ways 
    to achieve regulatory goals.
    
    List of Subjects in 7 CFR Part 353
    
        Exports, Plant diseases and pests, Reporting and recordkeeping 
    requirements.
    
    
    [[Page 1105]]
    
    
        Accordingly, we are amending 7 CFR part 353 as follows:
    
    PART 353--EXPORT CERTIFICATION
    
        1. The authority citation for part 353 continues to read as 
    follows:
    
        Authority: 7 U.S.C. 147a; 21 U.S.C. 136 and 136a; 44 U.S.C. 35; 
    7 CFR 2.22, 2.80, and 371.2(c).
    
        2. In Sec. 353.1, a definition of non-government facility is added, 
    in alphabetical order, to read as follows:
    
    
    Sec. 353.1  Definitions.
    
    * * * * *
        Non-government facility. A laboratory, research facility, 
    inspection service, or other entity that is maintained, at least in 
    part, for the purpose of providing laboratory testing or phytosanitary 
    inspection services and that is not operated by the Federal Government 
    or by the government of a State or a subdivision of a State.
    * * * * *
        3. In Sec. 353.7, paragraphs (a)(4), (b)(4), and (c)(4) are each 
    amended by adding a new sentence at the end of each paragraph to read 
    as follows:
    
    
    Sec. 353.7  Certificates.
    
        (a) * * *
        (4) * * * The Administrator may also authorize inspectors to issue 
    a certificate on the basis of a laboratory test or an inspection 
    performed by a non-government facility accredited in accordance with 
    Sec. 353.8.
    * * * * *
        (b) * * *
        (4) * * * The Administrator may also authorize inspectors to issue 
    a certificate on the basis of a laboratory test or an inspection 
    performed by a non-government facility accredited in accordance with 
    Sec. 353.8.
    * * * * *
        (c) * * *
        (4) * * * The Administrator may also authorize inspectors to issue 
    a certificate on the basis of a laboratory test or an inspection 
    performed by a non-government facility accredited in accordance with 
    Sec. 353.8.
    * * * * *
        4. A new Sec. 353.8 is added to read as follows:
    
    
    Sec. 353.8  Accreditation of non-government facilities.
    
        (a) The Administrator may accredit a non-government facility to 
    perform specific laboratory testing or phytosanitary inspection 
    services if the Administrator determines that the non-government 
    facility meets the criteria of paragraph (b) of this 
    section.1
    ---------------------------------------------------------------------------
    
        \1\ A list of accredited non-government facilities may be 
    obtained by writing to Phytosanitary Issues Management, PPQ, APHIS, 
    4700 River Road, Unit 140, Riverdale, MD 20737-1236.
    ---------------------------------------------------------------------------
    
        (1) A non-government facility's compliance with the criteria of 
    paragraph (b) of this section shall be determined through an assessment 
    of the facility and its fitness to conduct the laboratory testing or 
    phytosanitary inspection services for which it seeks to be accredited. 
    If, after evaluating the results of the assessment, the Administrator 
    determines that the facility meets the accreditation criteria, the 
    facility's application for accreditation will be approved.
        (2) The Administrator may deny accreditation to, or withdraw the 
    accreditation of, any non-government facility to conduct laboratory 
    testing or phytosanitary inspection services upon a determination that 
    the facility does not meet the criteria for accreditation or 
    maintenance of accreditation under paragraph (b) of this section and 
    has failed to take the remedial action recommended to correct 
    identified deficiencies.
        (i) In the case of a denial, the operator of the facility will be 
    informed of the reasons for the denial and may appeal the decision in 
    writing to the Administrator within 10 days after receiving 
    notification of the denial. The appeal must include all of the facts 
    and reasons upon which the person relies to show that the facility was 
    wrongfully denied accreditation. The Administrator will grant or deny 
    the appeal in writing as promptly as circumstances permit, stating the 
    reason for his or her decision. If there is a conflict as to any 
    material fact, a hearing will be held to resolve the conflict. Rules of 
    practice concerning the hearing will be adopted by the Administrator.
        (ii) In the case of withdrawal, before such action is taken, the 
    operator of the facility will be informed of the reasons for the 
    proposed withdrawal. The operator of the facility may appeal the 
    proposed withdrawal in writing to the Administrator within 10 days 
    after being informed of the reasons for the proposed withdrawal. The 
    appeal must include all of the facts and reasons upon which the person 
    relies to show that the reasons for the proposed withdrawal are 
    incorrect or do not support the withdrawal of the accreditation of the 
    facility. The Administrator will grant or deny the appeal in writing as 
    promptly as circumstances permit, stating the reason for his or her 
    decision. If there is a conflict as to any material fact, a hearing 
    will be held to resolve the conflict. Rules of practice concerning the 
    hearing will be adopted by the Administrator. However, withdrawal shall 
    become effective pending final determination in the proceeding when the 
    Administrator determines that such action is necessary to protect the 
    public health, interest, or safety. Such withdrawal will be effective 
    upon oral or written notification, whichever is earlier, to the 
    operator of the facility. In the event of oral notification, written 
    confirmation will be given as promptly as circumstances allow. This 
    withdrawal will continue in effect pending the completion of the 
    proceeding, and any judicial review thereof, unless otherwise ordered 
    by the Administrator.
        (3) The Administrator will withdraw the accreditation of a non-
    government facility if the operator of the facility informs APHIS in 
    writing that the facility wishes to terminate its accredited status.
        (4) A non-government facility whose accreditation has been denied 
    or withdrawn may reapply for accreditation using the application 
    procedures in paragraph (b) of this section. If the facility's 
    accreditation was denied or withdrawn under the provisions of paragraph 
    (a)(2) of this section, the facility operator must include with the 
    application written documentation specifying what actions have been 
    taken to correct the conditions that led to the denial or withdrawal of 
    accreditation.
        (5) All information gathered during the course of a non-government 
    facility's assessment and during the term of its accreditation will be 
    treated by APHIS with the appropriate level of confidentiality, as set 
    forth in the U.S. Department of Agriculture's administrative 
    regulations in Sec. 1.11 of this title.
        (b) Criteria for accreditation of non-government facilities. (1) 
    Specific standards for accreditation in a particular area of laboratory 
    testing or phytosanitary inspection are set forth in this part and may 
    be obtained by writing to APHIS. If specific standards for 
    accreditation in a particular area of laboratory testing or 
    phytosanitary inspection have not been promulgated by APHIS, and the 
    Administrator determines that accreditation in that area is practical, 
    APHIS will develop appropriate standards applicable to accreditation in 
    the area for which the non-government facility is seeking accreditation 
    and publish a notice of proposed rulemaking in the Federal Register to 
    inform the public and other interested persons of the opportunity to
    
    [[Page 1106]]
    
    comment on and participate in the development of those standards.
        (2) The operator of a non-government facility seeking accreditation 
    to conduct laboratory testing or phytosanitary inspection shall submit 
    an application to the Administrator. The application must be completed 
    and signed by the operator of the facility or his or her authorized 
    representative and must contain the following:
        (i) Legal name and full address of the facility;
        (ii) Name, address, and telephone and fax number of the operator of 
    the facility or his or her authorized representative;
        (iii) A description of the facility, including its physical plant, 
    primary function, scope of operation, and, if applicable, its 
    relationship to a larger corporate entity; and
        (iv) A description of the specific laboratory testing or 
    phytosanitary inspection services for which the facility is seeking 
    accreditation.
        (3) Upon receipt of the application, APHIS will review the 
    application to identify the scope of the assessment that will be 
    required to adequately review the facility's fitness to conduct the 
    laboratory testing or phytosanitary inspection services for which it is 
    seeking accreditation. Before the assessment of the facility begins, 
    the applicant's representative must agree, in writing, to fulfill the 
    accreditation procedure, especially to receive the assessment team, to 
    supply any information needed for the evaluation of the facility, and 
    to enter into a trust fund agreement as provided by paragraph (c) of 
    this section to pay the fees charged to the applicant facility 
    regardless of the result of the assessment and to pay the charges of 
    subsequent maintenance of the accreditation of the facility. Once the 
    agreement has been signed, APHIS will assemble an assessment team and 
    commence the assessment as soon as circumstances permit. The assessment 
    team will measure the facility's fitness to conduct the laboratory 
    testing or phytosanitary inspection services for which it is seeking 
    accreditation against the specific standards identified by the 
    Administrator for those services by reviewing the facility in the 
    following areas:
        (i) Physical plant. The facility's physical plant (e.g., laboratory 
    space, office space, greenhouses, vehicles, etc.) must meet the 
    criteria identified in the accreditation standards as necessary to 
    properly conduct the laboratory testing or phytosanitary inspection 
    services for which it seeks accreditation.
        (ii) Equipment. The facility's personnel must possess or have 
    unrestricted access to the equipment (e.g., microscopes, computers, 
    scales, triers, etc.) identified in the accreditation standards as 
    necessary to properly conduct the laboratory testing or phytosanitary 
    inspection services for which it seeks accreditation. The calibration 
    and monitoring of that equipment must be documented and conform to 
    prescribed standards.
        (iii) Methods of testing or inspection. The facility must have a 
    quality manual or equivalent documentation that describes the system in 
    place at the facility for the conduct of the laboratory testing or 
    phytosanitary inspection services for which the facility seeks 
    accreditation. The manual must be available to, and in use by, the 
    facility personnel who perform the services. The methods and procedures 
    followed by the facility to conduct the laboratory testing or 
    phytosanitary inspection services for which it seeks accreditation must 
    be commensurate with those identified in the accreditation standards 
    and must be consistent with or equivalent to recognized international 
    standards for such testing or inspection.
        (iv) Personnel. The management and facility personnel accountable 
    for the laboratory testing or phytosanitary inspection services for 
    which the facility is seeking accreditation must be identified and must 
    possess the training, education, or experience identified in the 
    accreditation standards as necessary to properly conduct the testing or 
    inspection services for which the facility seeks accreditation, and 
    that training, education, or experience must be documented.
        (4) To retain accreditation, the facility must agree to:
        (i) Observe the specific standards applicable to its area of 
    accreditation;
        (ii) Be assessed and evaluated on a periodic basis by means of 
    proficiency testing or check samples;
        (iii) Demonstrate on request that it is able to perform the tests 
    or inspection services representative of those for which it is 
    accredited;
        (iv) Resolve all identified deficiencies;
        (v) Notify APHIS as soon as possible, but no more than 10 days 
    following its occurrence, of any change in key management personnel or 
    facility staff accountable for the laboratory testing or phytosanitary 
    inspection services for which the facility is accredited; and
        (vi) Report to APHIS as soon as possible, but no more than 10 days 
    following its occurrence, any change involving the location, ownership, 
    physical plant, equipment, or other conditions that existed at the 
    facility at the time accreditation was granted.
        (c) Fees and trust fund agreement. The fees charged by APHIS in 
    connection with the initial accreditation of a non-government facility 
    and the maintenance of that accreditation shall be adequate to recover 
    the costs incurred by the government in the course of APHIS' 
    accreditation activities. To cover those costs, the operator of the 
    facility seeking accreditation must enter into a trust fund agreement 
    with APHIS under which the operator of the facility will pay in advance 
    all estimated costs that APHIS expects to incur through its involvement 
    in the pre-accreditation assessment process and the maintenance of the 
    facility's accreditation. Those costs shall include administrative 
    expenses incurred in those activities, such as laboratory fees for 
    evaluating check test results, and all salaries (including overtime and 
    the Federal share of employee benefits), travel expenses (including per 
    diem expenses), and other incidental expenses incurred by the APHIS in 
    performing those activities. The operator of the facility must deposit 
    a certified or cashier's check with APHIS for the amount of the costs, 
    as estimated by APHIS. If the deposit is not sufficient to meet all 
    costs incurred by APHIS, the operator of the facility must deposit 
    another certified or cashier's check with APHIS for the amount of the 
    remaining costs, as determined by APHIS, before APHIS' services will be 
    completed. After a final audit at the conclusion of the pre-
    accreditation assessment, any overpayment of funds will be returned to 
    the operator of the facility or held on account until needed for future 
    activities related to the maintenance of the facility's accreditation.
    
        Done in Washington, DC, this 5th day of January 1999.
    Craig A. Reed,
    Administrator, Animal and Plant Health Inspection Service.
    [FR Doc. 99-396 Filed 1-7-99; 8:45 am]
    BILLING CODE 3410-34-P
    
    
    

Document Information

Effective Date:
2/8/1999
Published:
01/08/1999
Department:
Animal and Plant Health Inspection Service
Entry Type:
Rule
Action:
Final rule.
Document Number:
99-396
Dates:
February 8, 1999.
Pages:
1098-1106 (9 pages)
Docket Numbers:
Docket No. 95-071-2
RINs:
0579-AA75: Phytosanitary Export Certification; Accreditation of Nongovernment Facilities
RIN Links:
https://www.federalregister.gov/regulations/0579-AA75/phytosanitary-export-certification-accreditation-of-nongovernment-facilities
PDF File:
99-396.pdf
CFR: (2)
7 CFR 353.8(b)(4)
7 CFR 353.1