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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.


04 May 2017, 14:30


04 May 2017, 17:30


Hong Kong, China

MD Seminar EU


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


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


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)*
*All seat reservation is subjected to advanced enrollment and on a first-come-first-served basis. SGS Hong Kong reserves the final right on any decisions without prior notice.
For more information, please contact:

Certification and Business Enhancement
Tel: (852) 2765 3620

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.