Triveritas France opened in 2006 strengthening Triveritas’ presence in mainland EU, providing clients with access to experts having both local and international knowledge in all aspects of Regulatory Affairs and clinical development.
The French team have valuable experience of the centralised and decentralised authorisation procedures, MRP and MRL submissions.
Added to this the location of the office in rural Alsace – with great access to key Investigators and opinion leaders in the clinical field, an abundance of types of farms and husbandry, and veterinary practitioners keen, experienced and trained in VICH GCP – makes Triveritas France an excellent choice for clinical projects.
The range of experience at Triveritas France includes many years gained working in the Animal Health industry – including at some of the “Top 10” companies in both France and the UK.
Excellent English is spoken fluently by all of the team, who expertly perform and manage projects in
the areas of Pharmacovigilance, Regulatory Affairs and VICH GCP clinical studies.