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Clinical Development

Well-planned, carefully managed veterinary clinical trials

As the world’s only combined global CRO/CDMO specialising in animal health, we have the unique expertise, scale, and agility to see your product smoothly through clinical development, so you can confidently prove its potential.

Veterinary clinical development:
A complex endeavour

Progressing your animal health product through target animal safety can be difficult, and demands significant time, resources, and expertise.

Key challenges include:

Regulatory
roadblocks
Veterinary medicine developers must deftly navigate complex and changing regulations that vary drastically by region and product type. Proceeding without the right knowledge can add significant time and costs to a clinical programme.
Logistical and
organisational complexity
Veterinary clinical trials have many moving parts. Keeping everything running smoothly means overcoming a variety of logistical and organisational challenges, including securing the right expert investigators in a timely fashion, and ensuring they have the resources they need to succeed.
Trial design and
data difficulties
Unveiling the true clinical value of your product hinges on suitable clinical trial design and expert statistical analysis of complex data sets. Getting these wrong can be the difference between programme success and failure.

Argenta: Smoothing your path to clinical development success

To bring an animal health product to market, you need the support of an animal health expert.

We’ll help you evaluate your product’s potential with expertly planned and managed pre-clinical and clinical studies in compliance with VICH-GCP, delivering results on time, within budget, and backed by the highest quality data.

Strategic direction and
regulatory management
Receive strategic direction from our experts, who have strong relationships with the European Medicines Agency (EMA), the European Food Safety Authority (EFSA), and the US Food and Drug Administration (FDA)’s Center for Veterinary Medicine (CVM). We help achieve alignment on critical study protocols for pre-clinical and clinical studies, so you can experience a seamless development journey.
An extensive network for
exceptional outcomes
Access Argenta's abundant clinical investigator network of the most skilled and knowledgeable clinical sites in Europe and the US. We also offer a full-service diagnostic laboratory for microbiology, virology, parasitology, and challenge preparation, with state-of-the-art equipment and an experienced, GCP/GLP-trained laboratory team.
Diverse species, indication,
and product type expertise
We can run clinical studies for any species (whether companion or production animals) for all indication areas and a plethora of products — including small molecule pharmaceuticals, biologics, feed additives, and medical devices.
Clinical development services

Our comprehensive clinical services include: 

  • Pre-clinical and clinical study design
  • Study protocol development
  • Application for clinical study permits and licences from regulatory authorities
  • Study site and associated study personnel recruitment
  • Monitoring
  • Data management
  • Quality assurance
  • Creation of study-specific materials through our pharmaceutical development teams
Other studies we can perform
  • Pilot clinical study (go/no go decision)
  • Post registration/marketing studies
  • Palatability studies
  • Prescription diet studies
  • Epidemiological studies

Approach your clinical trials with confidence

Ready to discover how our clinical solutions can support your product’s success?

Reach out to our knowledgeable clinical experts today
.

A solution for every step of the way

Argenta offers a full range of 'molecule to market' services to help advance your world-class animal health products. Wherever you are in your product development journey, Argenta can help.

Discover our full range of ‘molecule to market’ services: