Introduction The new Medical Devices Regulation (2017/745/ EU) (MDR) and the In Vitro Diagnostic Medical Devices Regulation (2017/746/EU) (IVDR) bring
As a part of the drug evaluation and approval reform in China, the enhanced Marketing Authorization Holder (MAH) system is
At the end of August, China’s legislature finally approved the long-awaited Drug Administration Law. Capping the dizzying regulatory reform since
“There is no point in stakeholders closing their eyes and pretending nothing is changing. We’re moving in the direction of
Abstract Across industries, digitization and the resulting increase in the access to data is changing the way organizations are serving
