The Global Regulatory Landscape – How to best comply?
- How do different regulatory requirements impact the global manufacturer?
- How can manufacturers efficiently fulfil different regulations with one approach?
- What are the real industry needs to be addressed?
- How can post-market activities be addressed by one holistic approach?
- Can Science of Patient Input (SPI) contribute to validating post-market feedback?
FACILITATED BY
OLIVER CHRIST | Global Managing Director, Medical Devices and IVD Consulting | NSF
PANELLISTS INCLUDE
PHIL BROWN | Director, Regulatory and Compliance | ABHI
GRAEME TUNBRIDGE | Senior Vice President, Global Regulatory and Quality, Medical Devices | BSI
JULIAN THORNS | Principal Consultant, Health Sciences EMEA | NSF