Consultation and Training in Medical Devices

Expert in ISO 13485, GDPMD, MDA Regulatory Requirements, CE marking, FDA related and Medical Device Related Requirements

Wednesday

GERAN UNTUK PERSIJILAN GDPMD



GERAN PERSIJILAN GDPMD  untuk
50 buah syarikat berkaitan Barangan Perubatan.

Hubungi segera:

e mail: sales.ummahsynergy@gmail.com


UMMAH SYNERGY VENTURES
03-3362 4502                                                       

Friday

MALAYSIA STANDARD ONLINE

CLIK HERE!

Latest List of CAB for GDPMD and Medical Device Registration


                                 

                           















                                 















                     
                                          

       


                       





























Thursday

NEW ISO 9001: 2015 UPDATE TRAINING


SEMINAR ON REGISTRATION OF MEDICAL DEVICE


SEMINAR ON REGISTRATION OF MEDICAL DEVICES
Registration of Medical Device is mandatory base on Medical Device Act 737, 2012.

Part II, registration of medical device and conformity assessment body

“Requirement for Registration of medical device
Part 5 (1) No medical device shall be imported, exported or placed in the market unless the medical device is registered under this Act.”
Overview:

Medical device product registration had been a hot topic among the stake holder ever since the Medical Device Act 737, gazetted and its requirement for all medical device related supplier or importer to register.

It had been a concern on the safety and performance of medical device being used and already widely circulated in the country.

Since no act had governing the supply and activity regarding the medical devices  supply chain, registration of medical device will be a move to ensure all medical device being circulated and distributed in the country  had undergone strict evaluation and monitoring, especially from the regulatory body, MDA.

The Topics:

  1. To make awareness of the registration approach
  2. Understanding the documentation requirement
  3. Compliance with product safety and performance
  4. Understanding CAB assessment requirements
  5. Consequences of product sold without registration
  6. The Fast Tract approach.
Speaker:

  1. MDA official (To be advice)
  2. CAB representative
  3. TBA
Who Should attend:
  1. Medical Device LAR
  2. Medical device Importer
  3. Medical Device distributor
  4. Medical Device Manufacturer

Target audience: 100 pax
Date and Time:

Date: 15/8/2015   Time: 9.30am - 1.00pm
Duration: 1/2 day
Location:
Ballroom, Hotel,  Shah Alam
Fee: RM 168 per pax.
E- mail your enquiry to:
sales.ummahsynergy@gmail.com @ booking at 03 7831 8502 (IZA)