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