CMC321 Consulting
Your Module 3, Our concern
Your Module 3, Our concern
Expertise in PHARMACEUTICAL REGULATORY AFFAIRS
About us
The firm relies on the bilateral expertise of consultantes who have worked in pharmaceutical laboratories and for ANSM, the French agency for drug and health-product safety.
Elisabeth RICCHI
Elisabeth is an expert in pharmaceutical regulatory affairs and pharmaceutical development with more than 25 years experience in pharmaceutical field: formulation development, Module 3 authoring, Module 3 assessment, all European procedures.
Bertille GAUTHIER
Bertille is an expert in pharmaceutical regulatory affairs and analytical chemistry with a 20- year experience in human and veterinary medicine
THEY TRUST IN US
Britol-Myers Squibb, UPSA, Sanofi Pasteur, Septodont, EUSA Pharma, Mayoly Spindler...
have already placed their trust in CMC321 Consulting and what do they say of our work ?
Rigorous approach, firm commitment to deadlines, well worked-out Dossiers, work compliant with our requirements
Good knowledge of our Dossiers, great responsiveness, appreciated availability
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