Digital FDA Submissions

Ensure complete compliance electronically

Get This Resource

Enhance your knowledge of product lifecycle management, commercialization and quality management.

Thanks for Learning with Us!

We’ve sent the resource you requested to your email. Enjoy!

Oops! Something went wrong while submitting the form.

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.

Related Resources


Engineer to Order Datasheet

The business model of engineer-to-order (ETO) companies continues to be jeopardized by shifting customer expectations...

Read More

Propel vs Agile

Product success requires a platform that is flexible, easy to use, integrated with the customer record, and fast to deploy.

Read More

Benefits of PLM and QMS Together

The rapidly changing business landscape means companies need to start pivoting and embracing customer-focused strategies...

Read More
Build better products faster.

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 solution

Get Started