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Eurofins Amatsigroup

(Headquarters) Parc de Génibrat
31470 Fontenilles

Phone: +33 (0)5 62 14 73 14


Eurofins Amatsigroup

Chemin de Mazerolles
64320 Idron

Phone: +33 (0)5 59 02 63 70


Eurofins Amatsigroup

7 Allée Isaac Newton
33650 Martillac

Phone: +33 (0)5 57 12 07 32


Eurofins Amatsigroup

17 Parc des Vautes
34980 Saint Gély du Fesc

Phone: +33 (0)4 99 58 38 60
Data Access: Click here


Eurofins Amatsigroup

Avenue Gay Lussac
ZI Artigues
33370 Artigues Pres Bordeaux 

Phone: +33 (0)5 57 02 19 20 

Eurofins Amatsigroup is a leading international Contract Development and Manufacturing Organization (CDMO) established in Europe.

Within Eurofins Amatsigroup, we provide high-quality, customized and cost-effective drug development solutions, integrated under one roof, to small biotech and major (bio) pharmaceutical customers.

Our innovative and flexible approach enables customers to speed up their drug development process, achieving key milestones in a timely manner.

Our services encompass:

  • Drug substance process development and manufacturing for biologics,
  • Formulation development and manufacturing of sterile and non-sterile clinical or small commercial batches
  • Clinical trial material (packaging & logistics).

A broad scientific, technical and regulatory expertise, combined with proactive troubleshooting skills, are the key assets of the company.

Our goal is to build a sustainable partnership with our customers to support their drug development pathway.


  • GMP compliant

Eurofins LC2

Z.A. du Charpenay
10 rue de l'Aqueduc
69210 Lentilly

Phone: +33 (0)4 74 72 17 77

Data Access: GEXWEB

Since 1995, LC² has developed expertise in primary packaging (blister packs and pillboxes), label design and printing, clinical labelling (booklet label up to 40 different languages, detachable flap label) and secondary packaging. This expertise is combined with an international logistics offer to investigative centres for multi-center clinical studies (reception and storage, distribution with control of the cold chain, management of returns and destruction) and a pharmaceutical release offer (import, Documentary, audits of manufacturing sites, and release of lots).


  • GMP GDP compliant (ANSM)


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