Clinical investigations of medical devices: What's new in 2024?
Today, new and exciting technologies emerge in the field of medical devices, and regulations are developing, too. Meanwhile, clinical data is becoming increasingly important.
MDR and regulation changes
Since its publication, knowledge and guidelines on how to implement the Medical Device Regulation (MDR) have grown rapidly. New essential guidelines from the Medical Device Coordination Group (MDCG) have been released, and everyone working with medical device studies should know about them. Keeping up-to-date with regulations and standards such as MDR and ISO 14155 is crucial for clinical investigations.
Join this bite-sized video training to learn about the key guideline changes for clinical investigations and other crucial developments in 2024! We are seeing ongoing pressure and no decrease in complexity to reach accordance with MDR, while the final deadlines are here.
In this 12-minute webinar, we will look into the following topics:
- What is new with MDCG 2024-3?
- Are more clinical investigations required?
- What is included in an effective Clinical investigation plan (CIP)?
- Why is clinical data now so important under MDR?