Home > Newsletters > International Medical Device Regulatory Monitor > Report Raises Questions of Eudamed’s Utility as Market Surveillance Tool
International Medical Device Regulatory Monitor
November 2012 | Vol. 20 No. 11
Report Raises Questions of Eudamed’s Utility as Market Surveillance Tool
The EU’s centralized medical devices database, Eudamed, contains incomplete information on devices and stakeholders, lacks transparency and is burdensome for competent authorities to use, a review by the European Commission concludes. Includes the full text of European Commission’s Review of EudaMed.
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