Nouveauté ! Développez votre produit SxMD avec un eQMS structuré comprenant des modèles SxMD prêts à être audités et conformes aux normes EU et US. En savoir plus !
Mastering EU MDR
Essential Strategies for Effective Risk and Document Management
Risk & Document management is an essential part of the MDR process.
Download this webinar to understand the risk management process, key requirements of MDR and best practices for compliance.
Key Takeaways:
How to adopt a risk based approach (Risk analysis)
How correct documentation can save time to market (New/Existing Products)
How Our Client (Early adopters) were able to save 6 months by leveraging the right tools
Key learnings from experts so you can ensure your product gets to market faster
Who should attend:
SxMD, SaMD, SiMD
Medtech companies within 25-500 employees
RA/QA
Software Engineers, Medtech, Regulatory Specialists
Thank you
A member of our team will be in contact within 48 hours to see how you enjoyed the webinar.