Sarah Elizabeth Morris - Comment

Document ID: FDA-2011-N-0447-0002
Document Type: Public Submission
Agency: Food And Drug Administration
Received Date: June 22 2011, at 12:00 AM Eastern Daylight Time
Date Posted: July 15 2011, at 12:00 AM Eastern Standard Time
Comment Start Date: June 20 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: August 19 2011, at 11:59 PM Eastern Standard Time
Tracking Number: 80e95ab7
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This is comment on Notice

Agency Information Collection Activities; Proposals, Submissions, and Approvals: Scientific and Technical Issues Related to Pharmaceutical Current Good Manufacturing Practice

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The guidance is intended to provide information to manufacturers of veterinary and human drugs, including human biological drug products, on how to resolve disputes of scientific and technical issues relating to CGMP. I think that this is a great proposal. People need to feel comfortable taking drugs and giving them to their loved ones and pets without worrying about scientific and technical issues going on with the drug.

Related Comments

Total: 1

Sarah Elizabeth Morris - Comment
Public Submission Posted: 07/15/2011 ID: FDA-2011-N-0447-0002

Comment Period Closed
Aug 19,2011 11:59 PM ET