98-29515. Development and Use of Guidances on Antimicrobial Drug Products; Draft Guidances for Industry on the Development of Antimicrobial Drug Products; Reopening of Comment Period  

  • [Federal Register Volume 63, Number 213 (Wednesday, November 4, 1998)]
    [Notices]
    [Page 59569]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-29515]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket Nos. 98N-0517 and 98D-0548]
    
    
    Development and Use of Guidances on Antimicrobial Drug Products; 
    Draft Guidances for Industry on the Development of Antimicrobial Drug 
    Products; Reopening of Comment Period
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice; reopening of comment period.
    
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    SUMMARY: The Food and Drug Administration (FDA) is reopening until 
    January 29, 1999, the comment period for two Federal Register notices 
    regarding guidance documents on developing antimicrobial drug products: 
    A notice requesting comment on the agency's process for developing and 
    using guidance documents on the development of antimicrobial drug 
    products (63 FR 39096, July 21, 1998) and a notice announcing the 
    availability of a general draft guidance for industry entitled 
    ``Developing Antimicrobial Drugs--General Considerations for Clinical 
    Trials'' and 17 draft guidances on developing antimicrobial drug 
    products to treat individual indications (63 FR 40532, July 29, 1998). 
    FDA is reopening the comment period for both notices to provide 
    interested persons additional time for review and comment.
    
    DATES: Written comments by January 29, 1999. General comments on agency 
    guidance documents are welcome at any time.
    ADDRESSES: Copies of the 18 draft guidances for industry are available 
    on the Internet at ``http://www.fda.gov/cder/guidance/index.htm''. 
    Submit written requests for single copies of the draft guidances to the 
    Drug Information Branch (HFD-210), Center for Drug Evaluation and 
    Research, Food and Drug Administration, 5600 Fishers Lane, Rockville, 
    MD 20857. Send one self-addressed adhesive label to assist that office 
    in processing your requests. Submit written comments on the draft 
    guidances to the Dockets Management Branch (HFA-305), Food and Drug 
    Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. 
    Comments are to be identified with the docket number found in brackets 
    in the heading of this document.
    
    FOR FURTHER INFORMATION CONTACT: Renata Albrecht, Center for Drug 
    Evaluation and Research (HFD-590), Food and Drug Administration, 5600 
    Fishers Lane, Rockville, MD 20857, 301-827-2336.
    
    SUPPLEMENTARY INFORMATION: In the Federal Register of July 21, 1998 (63 
    FR 39096), FDA's Center for Drug Evaluation and Research (CDER) 
    published a notice requesting comments on the development and use of 
    guidance documents for antimicrobial drug products. CDER requested 
    comment on the process the center is using to revise old and develop 
    new guidances for industry on the development of antimicrobial drug 
    products for the treatment of infections. In the Federal Register of 
    July 29, 1998 (63 FR 40532), CDER published a notice announcing the 
    availability of a general draft guidance for industry entitled 
    ``Developing Antimicrobial Drugs--General Considerations for Clinical 
    Trials'' and 17 draft guidances on issues related to developing 
    antimicrobial drug products to treat individual indications. The July 
    21 and July 29, 1998, notices invited interested persons to submit 
    written comments within 90 days.
        The agency has decided to reopen the comment period for both 
    notices until January 29, 1999, in response to requests for additional 
    time for public review and comment on the documents because of the 
    large number of draft guidances that were issued at one time.
        Interested persons may, on or before January 29, 1999, submit 
    written comments to the Dockets Management Branch (address above). Two 
    copies of any comments are to be submitted, except that individuals may 
    submit one copy. Comments are to be identified with the docket number 
    found in brackets in the heading of this document. The draft guidances 
    and received comments are available for public examination in the 
    Dockets Management Branch between 9 a.m. and 4 p.m., Monday through 
    Friday.
    
        Dated: October 28, 1998.
     William K. Hubbard,
     Associate Commissioner for Policy Coordination.
    [FR Doc. 98-29515 Filed 11-3-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
11/04/1998
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice; reopening of comment period.
Document Number:
98-29515
Dates:
Written comments by January 29, 1999. General comments on agency guidance documents are welcome at any time.
Pages:
59569-59569 (1 pages)
Docket Numbers:
Docket Nos. 98N-0517 and 98D-0548
PDF File:
98-29515.pdf