Rapidly changing technologies and access to software through connected platforms have blurred the lines between consumer and medical products.

This has historically led to some challenges for healthcare regulators and industry to recognize software as medical devices (SaMDs) and applicable regulatory requirements.

In this month's webinar, our Senior Consultants, Yervant Chijian and Jean Boudaud, will provide some insights on how to navigate this evolving topic.

Please take the opportunity to connect and share this video with your friends and family if you find it helpful.