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Home > Newsletters > International Medical Device Regulatory Monitor > Canada Delays STED Requirement for Device License Applications

International Medical Device Regulatory Monitor

July 2010 | Vol. 18 No. 7

Canada Delays STED Requirement for Device License Applications

Health Canada is postponing full implementation of summary technical documentation (STED) for premarket license applications for Class III and IV devices other than in vitro diagnostics (IVDs).

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