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