Getting to Yes from Regulators to Payers and Beyond - the Decision-Maker Gauntlet
After Yes - Navigating the Rules of the Road in Today's Marketplace
Regulatory, Quality and Good Manufacturing Practices
Case for Quality is a program developed under the auspices of the Medical Device Innovation Consortium (MDIC) where various stakeholders, including FDA and the Medtech industry have partnered to identify practices that lead to higher device quality. The program has been underway for several years and includes the CDRH Case for Quality Voluntary
Improvement Program (CFQ VIP), 18 companies and 51 facilities that undergo periodic assessment focused on practices that advance quality and safety and lead to better outcomes for patients.
Hear from leaders in the Case for Quality, who will discuss current program activities as well as what the future holds for CfQ. Get an agency perspective, including the benefits to companies participating in the program. Topics include: Qualifying to Participate in CfQ, Executive Engagement, the Voluntary Improvement Program, and others.