Explore our range of 1, 2 and 3-day courses covering the industry spectrum for your department - ensure you are prepared for the new Medical Device Regulation, and its implications on clinical evidence and surveillance requirements.
Evaluate the impact of regulatory changes on the medical device landscape to help you maintain compliance and manage transitions smoothly.
Explore the key challenges surrounding biocompatibility and how to overcome them.
Gain a comprehensive overview of the core components of risk management throughout the medical device lifecycle.
Learn the labelling and UDI requirements under the new MDR/IVDR and develop strategies for successful implementation.
Our online academies are perfect for busy professionals as they require just 2 hours per week of your time, and include an interactive forum for you to ask direct questions about challenges you are facing to expert course leaders.
Gain a comprehensive understanding of clinical evidence requirements throughout the life-cycle of a medical device product under the new MDR.
Gain an in-depth understanding of how the new Medical Device Regulation will apply to clinical investigations of medical devices.
Improve your understanding of the latest risk requirements and responsibilities outlined in the MDR.
Familiarise yourself with the updates to ISO 10993-1.