Medical Device Registration in UAE: Classification Requirements 1. Certificate from Country of Origin (Free Sale Certificate/CE/ISO) (No need to be legalized and FSC not to be issued from Chamber of…
Medical Device Registration in Saudi Arabia Click here to visit SFDA (Authority) website to learn more on medical device registration in Saudi Arabia. Labels to show the following: 1. The…
Free ISO 13485 Control of Documents Template Free ISO 13485 Control of Documents Template Use the link below to download this template. If the link does not work, email us here…
5159/ BYT-TB-CT Summary and Interpretation On the 28th Sep 2020, DMEC has just issued a letter on making public the price of medical equipment in a government portal. Please see…
Medical Device Registration in Taiwan Click here to visit the Taiwan FDA (authority) website. Requirements for QSD (Good Manufacturing Practice): 1. Quality Manual 2. SOP list 3. ISO 13485 certificate…