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In a competitive, regulated healthcare market, closed-loop quality management can provide the necessary advantage a medical device manufacturer needs to market new products quickly — while ensuring no quality has been compromised.
By closing the quality loop, you can design, build, deliver, and service high-quality products for global markets faster and with more functionality, while:
- Lowering overall risk
- Streamlining quality processes and manufacturing operations management
- Consolidating document control and data
- Ensuring regulatory compliance
From providing a complete set of thorough documentation to being your full-service validation provider, Propel provides the least burdensome approach to validation.
With smart factories on the rise, it's more important than ever to stay up to speed with the changing manufacturing jargon. Here's a handy list to keep around wherever you go.
Create, submit and audit MedWatch Form FDA 3500 submissions directly through Propel.
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
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