Medivecta gives sponsors access to pre-qualified testing sites in biologically relevant environments — with full study management, centralised QA, and sponsor-ready data packages that meet EMA, ECHA BPR, WHO PQ, and EPA standards.
A clear, managed process — so you know exactly what to expect at every stage. No surprises, no gaps.
Most testing organisations offer a site. We offer an established, governed network of qualified partners — combining scientific depth, regulatory expertise, and biologically relevant environments that no single facility can replicate. We have worked with our partners. We know their capabilities. And we manage every study end-to-end so sponsors get one contract, one accountable team, and data that stands up globally.
The life sciences industry faces a persistent problem: the best biological environments for testing are fragmented, under-governed, and inaccessible to sponsors.
Medivecta solves this — with an established network of partners we have worked with directly, governed under a centralised QA framework. We don't just connect sponsors to sites. We qualify them, harmonise their SOPs, manage the study, and guarantee the data output meets global regulatory standards. New partners are continuously onboarded against the same qualification criteria.
The result: data that stands up to global regulatory scrutiny at a cost that transforms early-stage development economics.
Discuss Your Study →Five capability domains. One governed network. Every study delivered to global regulatory standards.
Developing veterinary medicines, crop protection products, vector control tools, or clinical interventions — we deliver.
A selection of studies delivered through our network. Full programme details available under NDA for qualified sponsors.
Medivecta Lifesciences Global Partners is a regulatory testing partner built at the intersection of scientific expertise, regulatory knowledge, and global field networks.
We were founded to solve a structural problem in life sciences research: the most biologically relevant testing environments are fragmented, under-governed, and inaccessible to global sponsors. We have direct, hands-on experience working with testing partners across Sub-Saharan Africa and Europe — relationships built through delivered programmes, not cold outreach.
Our founding team brings expertise in veterinary science, regulatory entomology, medicines regulation, and global health programme delivery — with applied experience across Africa, Europe, and the UK, including delivered programmes across Wellcome Trust, JPIAMR, and Innovate UK.
We are not a generalist CRO and we are not a broker. We are a specialist testing partner with established field relationships, the scientific credentials to govern them, and the regulatory expertise to make the data they generate sponsor-ready for global markets.
Share your requirements. We'll come back with a clear proposal — timeline, cost, and regulatory pathway.
Whether you are a sponsor needing regulatory-grade testing data, a programme seeking field delivery in Sub-Saharan Africa, or a research institution interested in working with us — we want to hear from you.
All enquiries begin with a no-commitment conversation. We respond within 2 business days.