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Karine Pruvost is a skilled professional in the fields of regulatory affairs and quality management, currently serving as a Trainer for the IVDR course at CQHN asbl and as a QA Manager at Yellow5, where responsibilities include change and supplier management in accordance with ISO 13485:2016. Prior experience includes roles such as Regulatory Affairs Specialist at MEDI-LINE, Senior Regulatory Specialist at AXINESIS, and Regulatory & Quality Manager at Endo Tools Therapeutics, focusing on compliance with EU MDR and ISO standards, audit preparations, and technical file reviews. With a solid foundation in quality assurance, having previously worked for Baxter International Inc. and Laboratoire HUCKERT'S International, Karine has demonstrated expertise in maintaining quality systems, conducting audits, and implementing regulations. Educational qualifications include an MSc in Chemical Engineering from Imperial College London and an engineering degree from HEI - Hautes Etudes d'Ingénieur.