We are pleased to announce that we have completed a multi-year process to prepare for providing medical device certification services. Our experts, who have been involved in ensuring compliance with legal requirements and quality standards in the medical market for many years, have contributed significantly to this achievement.
We are proud of the experience and professionalism of our team, which will enable us to deliver services at the highest level. We have submitted our application along with the appropriate documentation for designation GCB as a notified body in accordance with Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices (MDR).
Obtaining MDR notification as well as our experts and auditors from around the world will give us the opportunity to certify many types of medical devices for customers regardless of their country of origin.
We encourage you to visit our website regularly, where we will keep you updated on our progress in obtaining MDR notification.
Keep your fingers crossed for us!
