PRISYM ID to speak at the MedTech Intelligence EU MDR - Requirements & Implementation
PRISYM ID will be presenting at this year’s MedTech Intelligence, EU MDR - Requirements & Implementation on July 17, 2019.
This complimentary, four-hour virtual conference, conducted by leading experts on EU MDR requirements and implementation, provides concise insights into key aspects of the regulation to help companies understand and plan for the impending changes.
Mark Cusworth, VP Research and Development at PRISYM ID will be speaking between 1:45 pm – 2:10 pm EST about EU MDR, UDI, Labeling – Regulatory Requirements:
- EU MDR label requirements compared with MDD and AIMDD
- Label – before and after EU MDR
- Comparison of EU MDR & FDA UDI
- EU MDR labeling solutions
The EU MDR poses tremendous economic and practical challenges for manufacturers. With deadlines looming, lingering ambiguities and limited availability of notified body support, companies are struggling with understanding the changes and implementing the right labeling solution. Please join Mark’ session to find out more.
You can also download our EU MDR – 10 Steps to Labeling Implementation guide:
About the speaker
Mark Cusworth, VP Research and Development, PRISYM ID
Mark has over 15 years of experience heading up a team providing off the shelf and tailored solutions to Life Science companies. During this time, he has seen many changes to the industry including significant tightening of regulations and challenges of globalization. His primary objectives are to target the ongoing investment in research, development and quality effectively and to lead the company in-house research and development.