In her latest article for IPI, Qinecsa President, Humaira Qureshi, addresses the practical challenges of integrating medical devices into pharmacovigilance portfolios. She explores the obligations of device manufacturers and offers insights on navigating the complexities of the European Medical Device Regulation (EU MDR).
“Understanding medical device regulations is essential for pharmacovigilance professionals seeking to master device vigilance compliance and operational excellence.”
Read the full article below:
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