Meriem Loukil is a seasoned pharmacovigilance assessor at ANSM Agence nationale de sécurité du médicament et des produits de santé since June 2012, specializing in the assessment of safety signals from post-marketing and clinical trials, as well as writing safety communications. Additionally, Meriem has experience as a medical devices and clinical trial assessor, evaluating protocols and adverse events. Previous roles include regulatory affairs trainer at Johnson & Johnson and sanofi-aventis. Meriem holds a Doctorate in Pharmacy and a Master's degree in regulatory affairs from Faculté de Pharmacie Châtenay-malabry, along with a Certificate of Statistical Studies Applied to Medicine from University Paris VI.

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Paris, France

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