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International Medical Device Regulatory Monitor
> IVD License Applications Focus of Health Canada Draft Guidance
International Medical Device Regulatory Monitor
September 2012
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20 No.
9
IVD License Applications Focus of Health Canada Draft Guidance
Manufacturers of Class III and Class IV in vitro diagnostic (IVD) devices will submit similar clinical and scientific information for summary technical document (STED)-based and non-STED-based license applications and amendments in Canada, according to two draft guidance documents.
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