Les membres / AMATSIGROUP

Groupe :

Services

Secteur :

Services

Activité principale :

Prestataire de services spécialisé dans les études de R&D sur le médicament à usage humain et vétérinaire.

coordonnées

Adresse :

Parc de Génibrat - 31470 FONTENILLES

Tél :

05 62 14 73 14

Fax :

05 62 14 73 10

Site :

http://www.amatsigroup.com/

Fiche de présentation

Amatsigroup is a leading partner in the early phases of pharmaceutical development thus making us an active contributor to health improvement. As a major European early CDMO (Contract Development Manufacturing Organization), we collaborate with small to large bio/pharmaceuticals companies offering integrated high-added-value drug development services.

Produits et services :

Amatsigroup is a leading partner in the early phases of pharmaceutical development thus making us an active contributor to health improvement. As a major European early CDMO (Contract Development Manufacturing Organization), we collaborate with small to large bio/pharmaceuticals companies offering integrated high-added-value drug development services. We apply a unique & innovative HighWay-to-Clinic™ approach delivering tailored  and troubleproof solutions which help advancing our client’s programs in a timely & cost effective manner. We support life science development through our scientific, technological & regulatory expertise. Transparency, team spirit, authenticity & trust are the core values that we share with clients. Our broad array of services encompasses: • Biologicals: Generation of cell banks & virus seeds, expression systems, bioprocess development, biomanufacturing, QC – QA & Release. • Bioservices: In Life studies (PK, ADME, residues, tolerance, efficacy studies…) & Bioanalysis. • Pharmaceutical Analysis Solutions: Analytical method development and validation, analytical support, stability studies, quality control (API, raw materials & drug products). • Formulation development & manufacturing: Bioavailability enhancement & drug release control; pilot & clinical batches manufacturing for parenteral, oral or topical forms. • Clinical trial supply: Packaging and Logistics: QP release, packaging, GMP storage, labeling & worldwide logistics. GLP & GMP environment (EU & US accreditations)