"Structure and objectives of the MDR"
Fundamentals of EU MDR and IVDR - Level 1 focuses on Reasons for the Medical Device Regulation, Structure and objectives of the MDR, Ability to identify the lifecycle of a device and the requirements of the various stages – premarket, design and development, product realization, and post market, How to transition from the old directives to the new regulation, Technical file requirements and reviews etc.
Timings08:30 AM - 04:30 PM (General)08:30 AM - 04:30 PM (General) | Entry FeesPaid Ticket Check Official Website |
Participants20 Delegates 5 Exhibitors Estimated Count | Category & TypeConferenceMedical & Pharma |
Editions30 - 31 Jan 2020 Interested07 - 08 Nov 2019 1st Edition Frequency Quarterly | Official LinksWebsite ContactsReport Error Claim this event |
Organizer Send Stall Book RequestComplianceOnline USATop Rated 356 events listed | |
User Community [ Users who have shown interest for this Event ]
Tracy Eberly
Regulatory Affairs at Fang Consulting, Ltd.
Minneapolis, United States
Aaditya Srikanth Sudarshan
R & D Engineer at Medtronic
Plymouth, United StatesWrite a Review
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Speakers (past edition)
Speaker
Kelly Eisenhardt
Co-Founder and Managing Director
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