Medical Innovation Exchange

MDIC

Regulatory Advocacy: Amplifying Your Voice

Regulatory Advocacy: Amplifying Your Voice     Medical devices and pharmaceuticals are heavily regulated. In the U.S., stakeholders have opportunities to communicate with regulators through pre-submission meetings, commenting on proposed regulations and draft guidances, and working with industry trade associations. But what is the right path for your particular company or concern? During the 2023 MedTech …

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PRI Establishes Working Group to Improve Medical Device Quality and Supply Chain Resiliency

PRI Establishes Working Group to Improve Medical Device Quality and Supply Chain Resiliency     The Performance Review Institute (PRI) has convened a new working group comprised of representatives from the medical device industry, government, and industry associations to identify and recommend best practices to improve medical device quality and enhance supply chain resiliency. The purpose …

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