This webinar was part of a HPRA Medical Devices webinars series held in November 2020 to provide information about the Medical Device Regulation (MDR) and the In Vitro Diagnostics Regulation (IVDR).
This webinar presentation covers two topics.
1:40 Avril Aylward provides an overview of the practical considerations relating to IVDR classification rules and some key implications for consideration.
23:44 Dr Philip Kelly provides an overview of the key requirements relating to IVDs and performance evaluation.
Негізгі бет IVDR update: IVD classification rules and performance evaluation
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