KMCRIC

Join us this June to help maximize your combination products’ lifespan and continue to deliver a quality drug-device product for your patients.

As the only peer-led community, we will bring in 100+ senior leaders from drug-device teams including the regulatory affairs, product development and quality to share their view and encourage collaborative efforts.

Aligning with industry trends, we will once again gather the community to explore and discuss:

◾How to handle and navigate the evolving regulatory landscape, especially EU MDR’s commercial implications on combination products in Japan and APAC

◾Design control and quality – how to collaborate with multiple teams for full oversight of LCM

◾When should you start an LCM initiative? Challenges with drug-device products.

◾Assessing next gen combination products opportunities to extend your product lifespan.