SONY DSCSONY DSCSONY DSCSONY DSCSONY DSCSONY DSC

Medical Devices Directives (93/42/EEC) and Technical File Preparation Workshop

30/05/13 - 31/05/13

The workshop was held for two days aiming familiarize delegates with the requirements of Directive 93/42/EEC as amended by Directive 2007/47/EEC. The training was designed for quality and regulatory professionals in their field with the technical documentation requirements of the Medical Device Directive 93/42/EEC, which includes the 2007/47 amendment. The event was organized by Singapore Manufacturer’s Federation, in collaboration with DH RegSys Pte Ltd and SGS International Certification Services Singapore Pte Ltd. Ms Tan Hwee Ee and Ms Lee Lai Mei were the key trainers for this workshop. 



← View all Past Events
OUR PARTNER
  • MD-CLINICALS Europe

    Route de Denges 28C
    1027 Lonay
    Switzerland

    Phone: +41 21 349 96 36
    Mobile: +65 98656730
    Fax: +41 21 349 96 37
    Site: www.md-clinicals.com
Call us at 6659 0979
Name*
Email*
Contact*
Enquiry*
Please complete the CAPTCHA.
− 6 = 0
I hereby give my consent to DH RegSys on sending SMS/MMS message, call, email and/or mail to my contact particulars provided herein.