Navitas Life Sciences On-Demand Webinar:  
Are you prepared for the new EU Medical Device Regulation (MDR) requirements? 

Join our Subject Matter Experts as they discuss the impact of EU MDR on Device and Combination Product Surveillance and Labeling.

This webinar explores:

  • The regulatory drivers and timelines 
    • Latest EU MDR Update 
    • Impact on product Surveillance and Labeling 
  • Implications of new regulatory requirements 
    • Surveillance Insights: Industry insights on implementing Device and Combination Product Surveillance Requirements 
    • Labeling Insights: Industry insights on implementing Device and Combination Product Surveillance Requirements 
  • Approach: Developing a holistic solution - People, Process, and Technology 
    • Governance can bind Process, Organization, and Compliance 
    • Procedures and Systems should allow for Transfer of Quality and Safety information with clear triggers 

Presenters:

Mayank Raizada
Senior Managing Consultant
Navitas Life Sciences

Olivier Goarnisson
Counsel
Sidley Austin LLP

Josefine Sommer
Senior Associate
Sidley Austin LLP

Please fill this form to view
First Name
✽
Last Name
✽
Business Email
✽
Company
✽
Job Title
✽
Country
✽
By submitting this form, I agree to receive email communications from Navitas Life Sciences. Privacy Policy

© 2020 Navitas Life Sciences | Privacy Policy