Pharmacovigilance companies monitor and assess the safety of medicines throughout clinical development and commercial use. Their services help pharmaceutical and biotechnology companies identify adverse effects, evaluate safety signals and meet ongoing reporting requirements.
This category includes companies working on:
Browse 34 UK pharmacovigilance companies below.
UK's largest early-phase clinical CRO specialising in first-in-human trials
Hammersmith Medicines Research is one of the largest early-phase contract research organisations in Europe, specialising in Phase I and early Phase II clinical trials of investigational medicinal products. Operating from a purpose-built 145-bed facility in West London, HMR provides fully integrated services from study…
Full-service CRO delivering clinical trial and regulatory support services
Optimapharm is a contract research organisation providing clinical trial management and observational study services to pharmaceutical, biotech and medical device companies. The company supports trials from Phase I through Phase IV, offering regulatory affairs, medical writing, clinical monitoring, data management,…
Full-service CRO for Phase I–IV pharmaceutical and device trials
Clinicology is a contract research organisation providing clinical trial management services to pharmaceutical, biotechnology, and medical device companies. Services span site startup, monitoring, project management, regulatory submissions, patient recruitment, medical monitoring, medical writing, and…
Specialist pharmacovigilance and drug safety services globally
PrimeVigilance is a contract research organisation specialising in pharmacovigilance and medical information services for pharmaceutical, biotechnology and medical device companies. The company delivers clinical safety monitoring, post-marketing surveillance, signal detection, benefit-risk management, literature…
Regulatory affairs, pharmacovigilance and compliance services for life sciences
ProductLife Group is a life sciences consulting and outsourcing company providing regulatory affairs, pharmacovigilance and quality services to pharmaceutical, biotechnology and medical technology organisations. Its teams prepare regulatory submissions, manage product registrations, monitor medicine safety and support…
Patient-controlled DNA biobank platform for precision prescribing insights
GeneHub is a London-based digital health company operating a patient-controlled biobank platform that rewards patients with free DNA tests and insights in exchange for sharing anonymised genetic data with researchers and clinicians. The platform aims to support precision prescribing, helping reduce adverse drug…
Generic and branded prescription medicines development and supply
Northumbria Pharma is a pharmaceutical company specialising in the development, manufacture, licensing, and supply of generic and branded prescription medicines across primary and secondary care. Its portfolio spans multiple therapeutic areas including rare diseases, neurology, respiratory, and oncology supportive…
Neuroimaging contract research organisation for clinical trial biomarker analysis
IXICO is a London-based imaging contract research organisation providing end-to-end neuroimaging services to biopharmaceutical companies conducting clinical trials in neurological diseases. The company collects, manages, and analyses MRI, PET, and SPECT imaging data from global trial sites, generating AI-driven…
GMP-certified pharmaceutical testing, regulatory and pharmacovigilance services
Sciom is a pharmaceutical services company providing integrated analytical, regulatory, quality and pharmacovigilance support to life sciences organisations. Operating from an MHRA-approved, GMP-certified facility, its services span analytical method development and validation, QC and microbiology testing, stability…
Real-world clinical data platform for life science research
Arcturis is a real-world data and evidence company that aggregates longitudinal, secondary-care patient records from a network of NHS hospitals into research-ready, regulatory-grade datasets. The platform combines structured and unstructured clinical data with molecular and genomic information, and is supported by HRA…
Full-service CRO specialising in oncology and rare diseases
Simbec-Orion is a full-service CRO providing Phase I to Phase IV clinical trial services, with specialist expertise in oncology, rare and orphan diseases, and clinical pharmacology. Its Merthyr Tydfil campus houses a 58-bed MHRA-accredited Phase I unit, Seirian Laboratories for central pathology and bioanalysis, IMP…
Regulatory affairs, quality assurance and clinical development consulting
G&L Scientific is a Belfast-founded regulatory affairs and quality assurance consultancy providing integrated product development and market access services to pharmaceutical, biopharmaceutical, and biotechnology clients globally. Services span CMC, clinical development, regulatory strategy and submissions,…
Specialist CRO for oncology, rare disease, and neurology clinical trials
Evestia Clinical is a global specialist contract research organisation providing full-service and functional clinical trial support to biotech and pharmaceutical companies. The company offers clinical operations, site and project management, regulatory affairs, biostatistics, pharmacovigilance, and medical writing…
Generic, branded and biosimilar medicines across global therapeutic areas
Viatris UK Healthcare is the UK subsidiary of Viatris Inc., a global pharmaceutical company formed in 2020 through the combination of Mylan and Pfizer's Upjohn division. Operating from sites in Hertfordshire, Cambridge, and Sandwich, Kent, the UK entity carries out formulation and device research and development,…