Mastering EU MDR
Essential Strategies for Effective Risk and Document Management
Risk & Document management is an essential part of the MDR process.
Join this webinar to understand the risk management process, key requirements of MDR and best practices for compliance.
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
Software Engineers, Medtech, Regulatory Specialists
A member of our team will be in contact within 48 hours to see how you enjoyed the webinar.