Navitas Life Sciences Live Webinar:  
Impact of EU MDR on Device and Combination Product Surveillance and Labeling 

Thursday, April 16, 2020 Time: 10:00 – 11:00 EST

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

This webinar will explore:

  • 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

Josefine Sommer
Senior Associate
Sidley Austin, LLP

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Live Webinar
Thursday, April 16, 2020 
Time: 10:00 – 11:00 EST 

 

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