Our company serves with its expert staff in the fields of chief auditor, committee membership and product expertise with more than 10 years of competence and notified body experience in the medical device sector.

Thanks to our long-term experience in the field of certification, strong technical infrastructure and trained team, we meet the needs of manufacturers with effective and permanent solutions. We provide domestic and foreign manufacturers in the medical device sector with the application, follow-up and after-sales services of the legal documents required to obtain free sales rights in European markets.

Through our solution partners, we provide the necessary services in the process of obtaining the EN ISO 13485:2016 and CE certificates required for the free circulation of all medical devices you produce in European markets. We manage your processes quickly and accurately by systematically organizing our service network and with the contributions of our solution partners.