Proven Ways to Overcome Today's Top Regulatory ChallengesEducation Sessions<img alt="" height="200" src="https://assets.swoogo.com/uploads/medium/3515330-65c260b7b0019.jpg" style="margin:10px;float:right;" width="300" /> The global orthopedic device regulatory landscape is a complex tapestry, and staying abreast of the latest developments can be challenging. This session provides practical advice on ways to respond to pressing issues and reviews priority topics for regulators in the U.S. and EU. Join industry experts for a comprehensive overview of the history, current guidance and outlook for Real World Evidence and MR testing and labeling. Gain insight into ways the Orthopaedic Alliance Roundtable provides timely and innovative solutions to barriers that impact the delivery of care. Learn about specific issues the working groups of the Orthopaedic Surgical Manufacturers Association (OSMA) are tackling and the resources you need to maintain market access for your company’s devices. Don’t miss out on critical regulatory updates shaping the future of medical device access and head home with the knowledge and connections you need to navigate the evolving landscape in the U.S. and European markets. This session is presented in collaboration with the Orthopaedic Surgical Manufacturers Association (OSMA), a device-company-led organization that works to enhance the implementation of global regulations and foster productive interactions between the orthopedic industry and regulators.

Description

The global orthopedic device regulatory landscape is a complex tapestry, and staying abreast of the latest developments can be challenging. This session provides practical advice on ways to respond to pressing issues and reviews priority topics for regulators in the U.S. and EU.

Join industry experts for a comprehensive overview of the history, current guidance and outlook for Real World Evidence and MR testing and labeling. Gain insight into ways the Orthopaedic Alliance Roundtable provides timely and innovative solutions to barriers that impact the delivery of care. Learn about specific issues the working groups of the Orthopaedic Surgical Manufacturers Association (OSMA) are tackling and the resources you need to maintain market access for your company’s devices. Don’t miss out on critical regulatory updates shaping the future of medical device access and head home with the knowledge and connections you need to navigate the evolving landscape in the U.S. and European markets.

This session is presented in collaboration with the Orthopaedic Surgical Manufacturers Association (OSMA), a device-company-led organization that works to enhance the implementation of global regulations and foster productive interactions between the orthopedic industry and regulators.