We’ve sent the resource you requested to your email. Enjoy!
Digital FDA Submissions allow medical device manufacturers to electronically create, submit and track progress with MedWatch Form FDA 3500A submissions directly through the Propel platform. Submissions and audit trails are fully integrated with product and quality capabilities, improving accuracy while streamlining the process.
Get unparalleled speed and flexibility throughout your entire value chain with streamlined collaboration between Engineering, Quality, Sales and Service – all on the world’s leading cloud solutionGet Started
We’ve received your contact request. A member of our team will be reaching out shortly to set up a time to talk via email.