Meeting the quality safety and performance requirements of medical equipment is already difficult and complicated, due to the multiplicity of standards and rules.

VIRA ANDISHEH PAD supports companies operating in medical device market through specialized training. In-house and private training is provided in the form of workshops and training courses for personnel and technical responsible staff of medical device companies.


Titles of training courses are as below:

Requirements and Implementation of Medical Device Regulation (MDR) For CE Marking
Requirements and Implementing ISO 13485:2016
Establishment and Updating Technical File
Risk Management for Medical Devices based on ISO 14971
Labeling and Packaging
Sterilization Validation