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GMDP-0093

Cheffe de projet en Affaires réglementaires

Verfügbar
5
Jahre Erfahrung
Regulatory Affairs
Spezialisierung
Frankreich
Standort
Über diesen Experten

Regulatory Affairs project manager specializing in CMC, pharmacovigilance, and pharmaceutical compliance. Experienced in AMM dossiers, change control, regulatory databases, and health authority interactions across vaccines, plasma-derived and dental products.

Kompetenzen

Experte
Regulatory Submissions Sterile manufacturing Plasma-derived medicinal products
Fortgeschritten
API Manufacturing Regulatory inspection support Liquid & semi-solid Oral solid dosage Biological & Immunological Testing SOP Writing & Review
Mittelstufe
Pharmacovigilance Annual Product Quality Review Deviation Management Computer system validation Stability Study Design & Execution
Grundkenntnisse
Packaging

Zertifizierungen

ICHM4QR1 & ICHM4QR2 Encadrement des avantages, loi anti-cadeaux et transparence Recherche impliquant la personne humaine (RIPH) Validation des systèmes informatisés (VSI) Pharmacovigilance Marketing digital Réglementation ICH - BPC et déclaration d'Helsinki Sensibilisation aux audits Life Science L'essentiel du dispositif médical et du médicament Marché des dispositifs médicaux : accès et remboursement Évaluation des connaissances réglementaires pour les personnes en charge de la promotion des médicaments Les bonnes pratiques cliniques Dangerous Goods Regulations Médiatrice de lutte anti-covid 19
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