Services

Preclinical & clinical services

Strategic planning, comprehensive study design, management and reporting of preclinical and clinical studies for development of veterinary medicines.

Preclinical and clinical study management
Our role

Scientific rigour at every study stage

Preclinical and clinical data form the backbone of any marketing authorisation application of veterinary medicinal products. Regivet provides expert guidance throughout the entire development programme, from study strategy and design to oversight, data management and reporting.

We help animal health companies generate robust efficacy and safety data that support successful regulatory submissions while avoiding unnecessary studies.
Our experts work closely with accredited CROs, veterinary clinics, farms and research institutions across Europe to ensure studies are delivered on time, within budget and in full compliance with regulatory expectations.

We speak the language of both regulators and veterinarians. That unique perspective allows Regivet to design studies that are not only scientifically sound, but also realistic, efficient and executable in everyday veterinary practice.

Strategic regulatory guidance
All target species
GCP and GLP compliant study management
Access to a European network of study sites
End-to-end data oversight
Cost-efficient development programmes
What's included

Services across the full development pathway

Study design & protocol development

Scientifically robust, regulatory-aligned study designs that generate the data you need — efficiently and without redundancy.

  • Regulatory strategy alignment
  • Study design optimization
  • Protocol writing (GCP/GLP)
  • Development of data collection forms

Study organization and monitoring

We speak both science and practice. Regivet turns study plans into studies that work in the real world.

  • Site selection, investigator recruitment and training
  • Trial clearance and IVP/CP coordination
  • Formulation of non-GLP test products
  • Laboratory and sample coordination

Data management and study reporting

End-to-end data management and reporting from collection through to regulatory-ready study reports.

  • Electronic data capture (EDC) or paper-based studies
  • Data cleaning and validation
  • Statistical analysis and reporting
  • GCP-compliant archiving

Every study. Every species. Every stage.

From laboratory and preclinical investigations to multicenter field studies, Regivet delivers end-to-end study support tailored to veterinary product development.

  • Clinical studies (from Pilot to Pivotal)
  • Bioequivalence and PK studies
  • Target animal safety studies, residue studies
  • Palatability and post marketing studies
Plan your study

Let's design your development programme

Tell us about your product and target species — we'll outline a preclinical and clinical programme that meets regulatory requirements without generating unnecessary data.

Get in touch