top of page

Market Authorisation of Medical Devices in European Union

EU market authorisation.jpg

Unimap in collaboration with MdDev  Sdn.Bhd. is pleased to invite you to our  training as follows:

Thursday ,7th March 2024, 9.00 am - 5.00 pm

Title: Market Authorisation of Medical Devices in European Union

Venue: Penang

Speakers : 
1.DR Vincent Lam Chee Choong
Vincent Lam is Senior Lead Auditor and Product Specialist for the Notified Body TÜV SÜD Product Service.In this role, he is responsible to establish and maintain device test programs for the assessment of specific medical devices to facilitate review of pre market regulatory requirements including the requirements of the European Notified Body conformity assessment scheme

2.Ir Dr Sasikala Devi A/P Thangavelu,

Professional Consultant & Trainer. Ex Officio Director of Policy, Code & Standard, Medical Device Authority, Malaysia
Registration fee: 

Fees: RM 1200/pax

Special rate available for Group Participation

Send your inquiry to  mddev.training@gmail.com  for HRDF claims

bottom of page