For our last webinar of the year, we are honoured to have a special guest: Francisco Vicenty, Program Manager, Case for Quality US FDA/CDRH/Office of Compliance join us.

The Case for Quality is a program developed under the auspices of the Medical Device Innovation Consortium (MDIC) where various stakeholders, including US 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 FDA’s leadership about the Case for Quality program. We 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.

Presenters: Arthur Brandwood CKC and Francisco Vicenty, US FDA

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