Tag: medicaldevice

Registration of Drug-device Combination Products

Standards

NMPA Notice on the Registration Requirements for Drug–Device Combination Products To strengthen the regulatory oversight and registration management of drug–device combination products, and in accordance...

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Medical Devices – USA/Europe Regulatory Updates round up – Sep 2021

Medical Device

EUROPE 1. Clarification on “first certification for that type of device” and corresponding procedures to be followed by notified bodies, in context of the consultation of the expert panel referred...

Europe, Europe FDA, Europe Medical Devices, Europe Regulatory Updates, FDA Updates, Medical quality, medicaldevice, Regulatory Updates, USA, Usa Medical Devices, USA Regulatory Updates

Tag: medicaldevice

Registration of Drug-device Combination Products

Medical Devices – USA/Europe Regulatory Updates round up – Sep 2021

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