New MDR 2017/745 certificates – week by week!
We are proud to announce that over one-third of Gofarm’s medical devices portfolio has received compliance certificates with EU MDR 2017/745 regulations!More certificates are on the way — our entire medical device portfolio (over 30 products!) is currently undergoing certification. We understand the challenges the medical device sector is facing across Europe — that’s why we ensure our products meet the highest quality standards and remain ready for safe market...
2024 SUMMARY IN GOFARM
With new energy and optimism we start 2025! We are exposed to risk and risk of an event and to further development as a substance expert of devices.We received a response - from our client, Partner, Supplier - for trust and control in 2024, which were approved by our goals and intention.See in a nutshell what infection in our company! 1. Regulatory Challenges and Successes In 2024, Gofarm focused on adapting its...
We are starting audits to certify Gofarm medical devices!
This important moment has finally arrived! We are pleased to announce that, as one of the first manufacturers of substance-based medical devices in Poland, today we are starting a series of certification audits for the first 13 medical devices from our portfolio for compliance with MDR 2017/745! We are waiting for 4 audits of the notified body PCBC S.A., thanks to which Gofarm products will soon obtain certificates of compliance. The first...
