US FDA 21 CFR 820.30 Design Control Requirements For medical device design, the US FDA is interested in what's the final fin... JassySam 1 year ago
Information about ISO 13485 - QMS Medical device manufacturer should appoint an experienced ISO13485 consulta... JassySam 1 year ago
Know more about CDSCO Import License in India Medical Devices entering to India must be in compliance with the Indian Med... JassySam 1 year ago
Know more about CE mark Certification CE Mark is mandatory to sell medical devices within any of the 32 European... JassySam 1 year ago
Regulation of FDA 510 k for Medical Device We help with the establishment enrollment and device listings to make suita... JassySam 1 year ago
CE mark Medical Device Certificate Consultant CE mark on a medical device or IVDs conforms that the device meets regulato... JassySam 1 year ago