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Public Workshop on Device Risk Management

12/07/2005

Federal Register Notice: FDA’s Dallas District Office, in collaboration with the FDA Medical Device Industry Coalition will hold a...

OMB OKs Info on MedWatch

12/07/2005

Federal Register Notice: FDA’s collection of information entitled "MedWatch: Food and Drug Administration Medical Products Reporti...

Guidance on Immune Globulin for Humoral Immunodeficiency

12/01/2005

Federal Register Notice: FDA is making available a draft document entitled Guidance for Industry: Safety, Efficacy, and Pharmacoki...

Info on Device Recall Sent to OMB

12/01/2005

Federal Register Notice: FDA submitted a proposed collection of information, “Medical Device Recall Authority — 21 CFR Part 810” t...

Address Change for ASTM

12/01/2005

Federal Register Final rule: FDA is amending its regulations to reflect a change in the address for the American Society for Testi...

Comments Sought on Focus Group Info

11/28/2005

Federal Register Notice: FDA is seeking public comment on a proposed collection of information on focus groups as used by the agen...

Schering-Plough Animal Changes Sponsor Address

11/28/2005

Federal Register Final rule: FDA is amending the animal drug regulations to reflect a change of sponsor's address for Schering-Plo...

Animal Drug Sponsor Name Changes

11/28/2005

Federal Register Final rule: FDA is amending the animal drug regulations to reflect a change of sponsor's name from Phoenix Scient...

FDA OKs Schering sNADA

11/28/2005

FDA OKs Schering sNADA

11/28/2005

Federal Register Final rule: FDA is amending the animal drug regulations to reflect approval of a Schering-Plough Animal Health Co...