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Tasnim Ben Amor is an experienced professional specializing in quality and regulatory affairs for medical devices, currently serving as the Head of Quality and Regulatory Affairs at OTR3 since November 2021. Prior experience includes a role as a Quality and Regulatory Affairs Consultant at EFOR, where responsibilities spanned implementing Quality Management Systems, technical file preparation for CE marking, and conducting audits. Tasnim has also worked as a Quality Engineer at Smiths Medical and a Quality Assurance Officer at Orgentec France, focusing on ISO certification and regulatory compliance. Educational qualifications include a Master's degree in Control and Quality from Université de Cergy-Pontoise and a Master 1 in Biochemistry and Cell Biology from CY Cergy Paris Université. Tasnim is currently pursuing certification as an Internal Auditor for ISO 13456:2016.