Compliance managers at prominent medical device companies are collaborating with the U.S. Food and Drug Administration to reinvent the methods for meeting quality regulatory standards. Supporting this vision, the next generation of cloud-based quality management systems brings modern, collaborative, web- and mobile-friendly productivity to help compliance professionals prepare for this new world.
A growing number of companies have joined the FDA Case for Quality Voluntary Medical Device Manufacturing and Product Quality Pilot. Officially launched in December 2017, the initiative now includes 24 facilities at 16 leading organizations such as Siemens, Medtronic, Baxter Healthcare, and Boston Scientific.
