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To ensure smoother transition of your Medical Device Quality Management System, we would like to invite you to join the Briefing Session for " the New Version of ISO 13485:2016 " on 26 April 2016. SEATS ARE LIMITED, RESERVE NOW!

Starts

26 Apr 2016, 14:30

Ends

26 Apr 2016, 17:00

Location

Hong Kong, China

INTRODUCTION

The new version of ISO 13485 is published on 1 March 2016. To ensure smoother transition of your Medical Device Quality Management System to be continuously complied with these new version requirements. We would like to invite you to join the briefing session for “the New Version of ISO 13485:2016” on 26 April 2016. SEATS ARE LIMITED, RESERVE NOW!

MAIN CONTENTS

  • ISO 13485:2016 vs ISO 13485:2003
  • ISO 13485:2016 vs ISO 9001:2015
  • Transition Plan

TARGET AUDIENCE

  • Medical Device Manufacturers & RA Specialist
  • Management Representative
  • Quality Management ; Engineering Management
  • Management of Operations, and
  • Logistics and Distribution Professional
  • Involving Parties in the Life Cycle of Medical Device

 

GENERAL INFORMATION

Date:   26 April 2016 (Tuesday)
Time:   14:30 – 17:00
Fee:   Free-of-charge
Language:   Cantonese 
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.