The Medical Devices team at BSI China recently hosted the BSI Medical Device Roadshow in Beijing to provide information to the regulatory community about some of the upcoming changes for the medical device industry.
BSI technical experts from across the world shared their knowledge on a range of topics including the new European Union Medical Device and IVD Regulations, clinical evaluation requirements and the global Medical Device Single Audit Program (MDSAP). The speakers discussed best practice and the latest expectations from the perspective of a leading certification body with the delegates, providing useful insight gained from an in-depth knowledge and real world experience of regulatory requirements.
The BSI experts were joined by guest speakers from a leading Chinese cardiovascular manufacturer and a global leading medical device manufacture, who provided their view of the regulatory changes and what it means for them.
The Forum attracted almost 80 delegates from medical device regulatory affairs, quality assurance and related consulting communities, all of who will be affected by the changes to market access requirements.
Explore our website to find out about the upcoming changes, and about events near you.
