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FDA Application

Federal Register
Friday November 6, 2009

Planning to Submit Comments?

Documents and comments received by the Division of Dockets Management may be posted on the Internet. Please do not include personal identifying information, i.e. date of birth, social security number, medical information, etc., in your correspondence.
Submit Electronic Comments

Documents are on display for public inspection at the Division of Dockets Management, 5630 Fishers Lane (Room 1061), HFA-305, Rockville, MD, 20852; 301-827-6860; TTY/TDD Users 1-800-735-2258.


FDA Federal Register Documents

NOTICES-FINAL GUIDANCES

Docket No. FDA-2009-D-0319, CDRH 200934.  Guidance for Industry and Food and Drug Administration Staff; In Vitro Diagnostic 2009 HINI Tests for Use in the 2009 H1N1 Emergency;.  Pages  57503-57504 [FR Doc. E9-26737]  [OFR PUB]

NOTICES

Docket No. FDA-2009-N-0507, OC 2009288.  Agency Information Collection Activities:Proposed Collection; Comment Request; Requirements for Submission of Labeling for Human Prescription Drug and Biologics in Electronic Format.  Pages  57491-57493 [FR Doc. E9-26760]  [OFR PUB] Comments due January 5, 2010

Docket No. FDA-2009-N-0506, OC 2009290.  Agency Information Collection Activities; Proposed Collection; Comment Request; Bar Code Label Requirement for Human Drug and Biological Products.  Pages  57495-57496 [FR Doc. E9-26850]  [OFR PUB] Comments due January 5, 2010


Table of Contents for Entire Federal Register
Friday, November 6, 2009 [Not Available]

 
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