In this webinar...
This webinar will provide thought-provoking discussions for the needed strategic planning for combination product regulatory compliance over the next 2-3 years due to the changing global regulatory landscape. The impending changes across the globe will increase the difficulty of navigating the regulatory landscape. When should companies start preparing for these changes? How can companies tailor their combination product launch strategies to meet these challenges? This presentation will lay out challenges and timelines of global regulatory changes, so senior management can appropriately develop their regulatory strategies to keep facilities in compliance and products on the market.
- Develop strategic priorities and plans for global regulatory compliance with regards to combination products with medical device constituent parts
- Discuss and plan for the challenges over the next couple of years
- Begin planning and performing Gap Analysis against these regulatory requirements
- Kim Trautman, MSc, Executive Vice President, Medical Device International Services, NSF International