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?


OLIVER CHRIST | Global Managing Director, Medical Devices and IVD Consulting | NSF


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