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    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

    Information about ISO 13485 - QMS

    Medical device manufacturer should appoint an experienced ISO13485 consulta...

    • JassySam

    Know more about CDSCO Import License in India

    Medical Devices entering to India must be in compliance with the Indian Med...

    • JassySam

    Know more about CE mark Certification

    CE Mark is mandatory to sell medical devices within any of the 32 European...

    • JassySam

    Regulation of FDA 510 k for Medical Device

    We help with the establishment enrollment and device listings to make suita...

    • JassySam

    CE mark Medical Device Certificate Consultant

    CE mark on a medical device or IVDs conforms that the device meets regulato...

    • JassySam