Propel's Digital FDA Submissions allow medical device manufacturers to:
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.
The lack of an efficient digital product thread significantly hinders company growth. Learn how to exceed revenue goals and customer expectations by better connecting your team and processes through a central technology solution.
Learn about what this integration does for you, and the associated capabilities and benefits.
Implement company-wide quality management processes that are tailored to your specific needs.
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