This course will provide Medical Technology (MedTech) industry professionals a chance to receive a quick yet comprehensive overview of regulatory and commercialisation of medical device and in vitro diagnostic device in Europe. It will also include market strategies, opportunities and challenges in the manufacturing and distribution of MedTech devices. Participants will gain valuable insight on medical devices with regulators, industry experts and academicians joining hands to share the global regulatory landscape and latest updates including the New CE MDR/IVDR , Clinical Evaluation, Brexit, Swixit and the challenges and experience of medical device startups in Medtech Industry. The course would also provide opportunities for like-minded MedTech professionals in exploring potential business collaboration.
Date: 28-29 September 2021
Venue: Online Platform (Zoom link TBC)
Gain valuable insights and experiences from the key respected speakers in the field to apply to your work/decision and preventing common mistakes.
Gain a comprehensive understanding on global regulatory landscape and latest updates including the new CE MDR/IVDR enforcement in May 2021/2022.
To hear about the market strategies, opportunities and challenges in the manufacturing and distribution. Networking with Medtech partners and industries, for potential collaboration.