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