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 group includes products from the ENT line, e.g. sea water for the nose, vaginal gel or honey syrup for dry and wet cough.
All of our medical products are already in a transitional period and our clients can safely sell them!
We expect certificates in a few months! The next group of products will be certified in 2025!
