Walid Deghi

Clinical Rgulatory Affairs Officer @Lysarc

Lyon, FR

Prepare, submit, and track authorization requests for clinical studies and substantial modifications with regulatory authorities and ethics committees in France and Belgium.• Coordinate regulatory submissions and provide compliance support for international studies conducted or supported by LYSARC.• Optimize regulatory timelines by minimizing review and approval delays and keeping project teams informed of progress.• Monitor regulatory developments in France, Belgium, Europe, and ICH, providing expert guidance on clinical study regulations.• Maintain and update internal regulatory documentation, ensuring compliance with current guidelines.• Revise and implement standard operating procedures (SOPs) and regulatory documents.• Act as the regulatory representative within project teams, ensuring adherence to legal and ethical standards.

Université Alger I, Faculté de Médecine

Docteur en pharmacie

Lycée De La Cité Diplomatique

Baccalauréat - sciences expérimentales - Mention Bien

UVSQ Université de Versailles Saint-Quentin-en-Yvelines

Master 2 Coordinateur d'Études dans le Domaine de la Santé (CEDS)

Université Paris-Saclay

Master 1 méthodes en santé publique