Seminar - The EU New Medical Device Regulation for MDR & IVDR
About
Join our seminar on 8 May, where our industry experts will provide an in-depth technical presentation and analysis on the new EU regulations for MDR & IVDR and its impact upon the implementation.
Starts
04 May 2017, 14:30
Ends
04 May 2017, 17:30
Location
Hong Kong, China
INTRODUCTION:
The final versions of the European Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Device Regulations (IVDR) had just been released by the European Council. On 7 March 2017, the European Council had voted to adopt the MDR and the IVDR. On 5 April 2017, the European Parliament endorsed the new MDR and IVDR. According to the schedule, the MDR and the IVDR could be published in May 2017 and enter into force in June 2017. Learn more
SEMINAR HIGHLIGHTS:
Introduction to new MDR and IVDR
- Changing from directive to regulation
- Legislation process
- Transition timeline
- Strategies for the new MDR and IVDR
Main changes
- New requirements
- Clarification of existing requirements
- Strengthen the post market control
SEMINAR DETAILS:
| Date: | 4 May 2017 (Thur) |
| Time: | 2:30pm - 5pm |
| Fee: | Free-of-charge |
| Language: | Cantonese (with English materials) |
| Venue: | 17/F, The Octagon, No.6 Sha Tsui Road, Tsuen Wan, N.T. |
| Quota: | 40 (Max. 3 participants per company)* |
Certification and Business Enhancement
Tel: (852) 2765 3620
Email: hk.cbe@sgs.com
About SGS
SGS is the world’s leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 90,000 employees, SGS operates a network of over 2,000 offices and laboratories around the world.