With more regulatory guidance for software and apps becoming available, it is imperative you understand how to classify your product so that you can apply the regulatory guidelines which concern it.
Build upon the knowledge of the Medical Device Regulation with two online courses designed to build your knowledge in software and apps:
1. Navigating the Regulations for Health Apps and Medical Device Software
2. Applying the Regulations for Health Apps and Medical Device Software
Led by Koen Cobbaert, learn from a regulatory expert in the field. Koen has co-written MEDDEV 2.1/6, MDCG 2011 - 11 and published guidance on the use of IEC 62304. Koen has extensive knowledge in this area. With MDTI's online academies, you will obtain direct contact with Koen ensuring any queries you have relating to the course material will be addressed throughout the course.
Purchase a place on both online academies and get 20% off, saving you a total of £258 + VAT. Attending both courses will provide you with a complete understanding of the regulatory requirements for health apps, how to apply them to your product and how to ensure patient safety.