Exchange ideas with your colleagues about the issues you face in validating software in your context.
Whether you manage manufacturing software, clinical data management or safety data management applications, or design instruments and devices with embedded software, this board is set up for you.
Feel free to post your comments in any of the topic areas we've set up. There's no need to join anything or sign your name, though you're welcome to enter your name and contact information if you would like other users to follow up with you directly. Of course, please observe all standards of professional courtesy (any posts we determine to be abusive, offensive, or threatening will be removed).
If you feel the Discussion Board needs a topic area beyond what we've set up, please send a request to tonyraymond@newharborsqa.com
The discussion board is hosted through the resources of the Medical Development Group, and co-moderated with ShoeBar Associates.
Take me to the board: FDA-Regulated Software Discussion Board
