Rx Surveillance User Fee Proposal Is Premature; PhRMA Responds To JAMA

Discussion of ways to fund expanded post-marketing surveillance activities by FDA should await a clear assessment of the extent of the problem, the Pharmaceutical Research & Manufacturers of America said in response to a May 20 Journal of the American Medical Association article entitled "Time To Take Action on Drug Safety."

Pink Sheet Podcast

Learn what's happening at the US FDA. On the go.

Derrick Gingery and the team bring you a weekly "Drug Fix".

More from Archive

More from Pink Sheet