Through a dedicated veterinary preclinical and clinical department, Cebiphar offers a wide range of services for the development of veterinary drugs, biological, zootechnical and food products. Field studies are conducted on farm animals and pets according to GCP principles.

Field clinical trials

  • Efficacy studies (for registration or post-marketing purposes)
  • Safety studies
  • Palatability studies (for pharmaceuticals, food supplements, additives…)
  • Microbiological studies: identification of field strains, MIC, field strains collection

Our services

  • Consulting and operational support
    • Development strategy for veterinary medicinal products
    • Study design: sample size determination, blinding, randomisation, determination of the reference product
    • Writing of protocols
    • Case Report Form preparation
    • Declaration of the clinical trial to regulatory agencies
    • Procedures for importing products for clinical trials
    • Selection of investigators and clinical sites
    • Training of investigators and co-investigators
    • Monitoring: regular on-site visits
    • Management of centralised laboratories
    • Pharmacovigilance during study
    • Collection and verification of data, queries
    • Statistical analysis, interpretation of results
    • Report writing
  • Distribution of products

    Our management and distribution of medicinal products for clinical trials is GMP compliant (ANSES):

    • Import and receipt of products
    • Storage under controlled conditions
    • Supply of authorised reference products
    • Distribution, collection, accounting and disposal of test products

Our Quality Assurance department is involved at every stage of the study (audit of the protocol, raw data and report).

Alongside the studies, Cebiphar ensures regulatory consultancy: audit of dossiers, bibliographic studies, registration support, writing of part III and IV.