This e-course provides a solid introduction to the key steps involved in bringing a medical device to market. It covers the essentials of the development process, incorporating interactive elements and knowledge checks to enhance your learning experience. View full course information
This course is aimed at those with regulatory experience in pharmaceuticals who wish to deepen their knowledge of the medical device aspects of combination products (drug-device). It consists of an e-course and an on-site session, providing key insights into the EU regulations for combination products. View full course information
Learn the essential requirements for ensuring that medical devices meet usability standards in Europe and the United States. This course provides insights on how to practically apply the regulations to ensure compliance and successfully launch your product on the market. View full course information