Clinical Trial Site Budgeting –Risk Mitigation or Budget Control?
Join NAMSA for a webinar that will highlight clinical trial site budgeting as both a risk mitigation strategy and an approach for sponsors to standardize site costs.
China: Key Regulatory Changes from 2022 and Look Ahead to 2023
Get the latest on NMPA’s updated guidance for the clinical evaluation of medical devices.
Navigating Trends and Best Practices For Cardiovascular Device Development
Join NAMSA and the FDA as they present a webinar on the Accreditation Scheme for Conformity Assessment (ASCA) Pilot Program, a first-of-its-kind conformity assessment program created by the U.S. FDA.
AdvaMed State Policy Briefing – Extended Producer Responsibility (EPR) – Environmental Sustainability and Recycling in Medtech
AdvaMed held a panel discussion with two member company experts on product stewardship and environmental sustainability.
Medtech Coverage, Coding and Reimbursement 101 and 201 Workshops
Learn the basic principles of how medical technologies are covered and paid by insurers and the challenges medtech companies face.
2023 Medical Device Submissions Workshops
These workshops will give you access to real-world case studies, tips and best practices directly from FDA and industry experts.
