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]

