97-27586. Hedviga Herman; Debarment Order  

  • [Federal Register Volume 62, Number 201 (Friday, October 17, 1997)]
    [Notices]
    [Page 54117]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 97-27586]
    
    
    
    [[Page 54117]]
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 95N-0070]
    
    
    Hedviga Herman; Debarment Order
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: The Food and Drug Administration (FDA) is issuing an order 
    under the Federal Food, Drug, and Cosmetic Act (the act) permanently 
    debarring Ms. Hedviga Herman, 1326 42d St., Brooklyn, NY 11219, from 
    providing services in any capacity to a person that has an approved or 
    pending drug product application. FDA bases this order on a finding 
    that Ms. Herman was convicted of a felony under Federal law for conduct 
    relating to the regulation of a drug product under the act. Ms. Herman 
    has failed to request a hearing and, therefore, has waived her 
    opportunity for a hearing concerning this action.
    
    EFFECTIVE DATE: October 17, 1997.
    
    ADDRESSES: Application for termination of debarment to the Dockets 
    Management Branch (HFA-305), Food and Drug Administration, 12420 
    Parklawn Dr., rm. 1-23, Rockville, MD 20857.
    
    FOR FURTHER INFORMATION CONTACT:  Christine F. Rogers, Center for Drug 
    Evaluation and Research (HFD-7), Food and Drug Administration, 5600 
    Fishers Lane, Rockville, MD 20857, 301-594-2041.
    
    SUPPLEMENTARY INFORMATION:
    
    I. Background
    
        On September 23, 1994, the United States District Court for the 
    District of Maryland entered judgment against Ms. Hedviga Herman for, 
    among other counts: (1) One count of introducing adulterated drugs into 
    interstate commerce, a Federal felony offense under 21 U.S.C. 331(a) 
    and 333(a)(2); (2) one count of introducing unapproved new drugs into 
    interstate commerce, a Federal felony offense under 21 U.S.C. 331(d) 
    and 333(a)(2); and (3) one count of obstruction of an agency 
    proceeding, a Federal felony offense under 18 U.S.C. 1505.
        As a result of these convictions, FDA served Ms. Herman by 
    certified mail on February 20, 1996, a notice proposing to permanently 
    debar her from providing services in any capacity to a person that has 
    an approved or pending drug product application, and offered her an 
    opportunity for a hearing on the proposal. The proposal was based on a 
    finding, under section 306(a)(2)(B) of the act (21 U.S.C. 
    335a(a)(2)(B)), that she was convicted of a felony under Federal law 
    for conduct relating to the regulation of a drug product. Ms. Herman 
    was provided 30 days to file objections and request a hearing. Ms. 
    Herman did not request a hearing. Her failure to request a hearing 
    constitutes a waiver of her opportunity for a hearing and a waiver of 
    any contentions concerning her debarment.
    
    II. Findings and Order
    
        Therefore, the Director, Center for Drug Evaluation and Research, 
    under section 306(a)(2)(B) of the act, and under authority delegated to 
    her (21 CFR 5.99), finds that Ms. Hedviga Herman has been convicted of 
    a felony under Federal law for conduct relating to the regulation of a 
    drug product.
        As a result of the foregoing finding, Ms. Hedviga Herman is 
    permanently debarred from providing services in any capacity to a 
    person with an approved or pending drug product application under 
    section 505, 507, 512, or 802 of the act (21 U.S.C. 355, 357, 360b, or 
    382), or under section 351 of the Public Health Service Act (42 U.S.C. 
    262), effective October 17, 1997 (sections 306(c)(1)(B) and 
    (c)(2)(A)(ii) and 201(dd) of the act (21 U.S.C. 321(dd))). Any person 
    with an approved or pending drug product application who knowingly uses 
    the services of Ms. Herman, in any capacity, during her period of 
    debarment, will be subject to civil money penalties (section 307(a)(6) 
    of the act (21 U.S.C. 335b(a)(6))). If Ms. Herman, during her period of 
    debarment, provides services in any capacity to a person with an 
    approved or pending drug product application, she will be subject to 
    civil money penalties (section 307(a)(7) of the act). In addition, FDA 
    will not accept or review any abbreviated new drug applications 
    submitted by or with the assistance of Ms. Herman during her period of 
    debarment.
        Any application by Ms. Herman for termination of debarment under 
    section 306(d)(4) of the act should be identified with Docket No. 95N-
    0070 and sent to the Dockets Management Branch (address above). All 
    such submissions are to be filed in four copies. The public 
    availability of information in these submissions is governed by 21 CFR 
    10.20(j). Publicly available submissions may be seen in the Dockets 
    Management Branch between 9 a.m. and 4 p.m., Monday through Friday.
    
        Dated: October 1, 1997.
    Janet Woodcock,
    Director, Center for Drug Evaluation and Research.
    [FR Doc. 97-27586 Filed 10-16-97; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Effective Date:
10/17/1997
Published:
10/17/1997
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
97-27586
Dates:
October 17, 1997.
Pages:
54117-54117 (1 pages)
Docket Numbers:
Docket No. 95N-0070
PDF File:
97-27586.pdf