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Our Services

As an animal health consultancy specialising in VICH GCP clinical studies, we understand the importance of maintaining the highest standards of quality.

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EXPLORE OUR ALL-INCLUSIVE OFFERINGS

Our Services

The VICH GCP Consultancy collaborates with established industry experts to build a consortium of key study participants tailored to meet the specific requirements of each study. Leveraging this established network and collaboration, the VICH GCP Consultancy designs, conducts, and manages clinical studies that adhere to the rigorous guidelines established by VICH GCP. 


This ensures the production of meticulously refined and validated study reports, ready for submission to regulatory authorities.


Explore our all-inclusive offerings, including monitoring, quality assurance, project management, and protocol/report writing, tailored for the animal health industry.

Monitoring

Our all-inclusive monitoring services encompass protocol quality control, site screening, study set-up, electronic data capture user acceptance testing, real-time oversight, study close-out, and data quality control and validation checks, ensuring adherence to VICH GCP standards and the seamless conduct of veterinary clinical studies.

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Quality Assurance

This service includes conducting an unbiased independent assessment of quality including audits of the following: protocol, data, data entry, study files, investigator sites, statistical and final study reports.

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Study Management

We specialise in comprehensive study management services, from facility inspections to protocol reviews and in-phase sponsor representative visits, ensuring regulatory compliance and study success from concept to report.

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Protocol & Report Writing

The VICH GCP Consultancy takes great pride in delivering exceptional quality protocols and reports that meet the strict standards of both our clients and regulatory agencies across the world. Our approach is characterised by a strong focus on collaboration, communication and timely delivery. With extensive knowledge of both pre-clinical and clinical studies, the ability to translate complex scientific language into structured and systematic protocols for use in the field, and then take the data pack and generate first-pass regulatory compliant reports is essential to streamline the drug development process and minimise delays in bringing new veterinary medicines to market.

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Interested in our services? We’re here to help!

Reach out today so that we can assess your needs and offer the ideal solution for you.

Contact Our Team
WE UNDERSTAND THE IMPORTANCE OF MAINTAINING THE HIGHEST STANDARDS OF QUALITY IN ANIMAL HEALTH.
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