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Clinical evaluation strategy for Medical Device Software certification under MDR/IVDR

Outscoring your regulatory affairs activities? Why?

STARoDub Outing 2023

Toxicological risk assessment of mutagenic impurities

Is it possible to optimize development process of your medicinal product?

STARoDub @ BioEurope Munchen and Nordic Life Science (NLS) Days in Copenhagen

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Valentyna Starodub
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