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Info on Physician Survey Sent to OMB

07/19/2007

Federal Register Notice: FDA’s proposed collection of information, “FDA Survey of Physicians' Perceptions of the Impac...

Brethine Not Withdrawn For S&E

07/19/2007

Federal Register Notice: FDA determines that Brethine (terbutaline sulfate) injection was not withdrawn from sale for reasons of s...

Comments Sought on Harmonized Device Proposals

07/13/2007

Federal Register Notice: FDA is making available and requesting comments on several proposed and final documents that have been pr...

ICH Guidance on the Pharmaceutical Quality System

07/13/2007

Federal Register Notice: FDA is making available a draft guidance entitled Q10 Pharmaceutical Quality System prepared under the au...

Guidance on Decorative/Non-corrective Contacts

11/27/2006

Federal Register Notice: FDA is making available a document entitled Guidance for Industry, FDA Staff, Eye Care Professionals, an...

Dispute Panel to Discuss Acorn Device

11/27/2006

Federal Register Notice: FDA’s Medical Devices Dispute Resolution Panel of the Medical Devices Advisory Committee will meet...

Comments Sought on E-submissions to CVM

11/08/2006

Federal Register Notice: FDA is seeking comments on extending Office of Management and Budget (OMB) approval on the existing repo...

Comments Sought on E-mailing a Study Protocol

11/08/2006

Federal Register Notice: FDA is seeking public comment on extending OMB approval of existing reporting requirements for the infor...

Comments Sought on Electronic Meetings Requests with CVM

11/08/2006

Federal Register Notice: FDA is seeking comments on extending Office of Management and Budget (OMB) approval of existing reportin...

FDA Submits Info on Device Inspections to OMB

11/03/2006

Federal Register Notice: FDA’s proposed collection of information, "Medical Devices: Inspection by Accredited Persons Progr...