CaptureHelp FDA Improve FDA MedWatch Forms

MedWatch is FDA gateway for clinically important safety information and reporting serious problems with human medical products

  • Physicians and Consumers can report unexpected side effects, adverse events, or other problems through MedWatch program
  • Report adverse events, product problems, errors with use,  evidence of therapeutic failure is suspected or identified

FDA is seeking comments to help improve adverse event information collection

  • Forms 3500, 3500A and 3500B

regulations.gov


Image credit: FDA


Leave a Reply


Fill in your details below or click an icon to log in:

WordPress.com Logo



You are commenting using your WordPress.com account.
Log Out / 
Change )

Google photo



You are commenting using your Google account.
Log Out / 
Change )

Twitter picture



You are commenting using your Twitter account.
Log Out / 
Change )

Facebook photo



You are commenting using your Facebook account.
Log Out / 
Change )

Connecting to %s