throughout the product life cycle
We have access to a global network of more than 100 industry experts with wide-ranging specialisms so if you do not see your chosen topic in this catalogue, simply get in touch and we will be happy to develop the training for you.
Understanding the Medical Device Regulation
Understanding the European IVD Regulation
EU Regulatory Affairs for Medical Devices
US Regulatory Affairs for Medical Devices
Regulatory Affairs in Latin America for Medical Devices
Medical Devices in the MENA Region
Gaining Marketing Authorisations in the CIS for Medical Devices
Post Market Surveillance and Vigilance Strategies
Medical Device Regulatory Project Management
Understanding Biocompatibility for Medical Devices
Drug/Device Combination Products
Understanding ISO 13485:2016 and the Medical Device Single Audit Programme
Understanding ISO 14155:2019 Key Updates for Clinical Investigations
Navigating and Applying the Regulations for Health Apps and Medical Device Software
Risk Management for Medical Devices
Understanding Clinical Evaluations, Investigations and Post Market Clinical Studies
Brexit: The Challenges and Impact on the Medical Device Industry
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