NMPA Regulation Revision
China’s National Medical Products Administration (NMPA) published the revised regulation on the Supervision and Administration of Medical Devices on 19 March 2021
EU Regulatory Basics
Gain a latest insight into the European regulatory framework for medical devices focusing on legal basis, technical documentation and clinical evaluation.
Database Updated
European and Chinese regulatory guidelines for medical devices are fully updated at HengRy Intelligence Database.
Clinical Evaluation
Gain a fundamental insight into the European regulatory Affairs focusing on clinical evaluation.
Technical Doc.
Gain a fundamental insight into the European regulatory framework for medical devices with a focus on technical documentation.
