Medicines Evaluation Unit
Medicines Evaluation Unit (MEU) is a UK-based, MHRA-accredited Phase I contract research organization (CRO) and IQVIA subsidiary specializing in early phase clinical trials across respiratory, dermatology, cardiovascular, inflammatory, and diabetes indications, operating a 36-bed facility in Manchester and a Salford Quays satellite.
- Company typePrivate
- Founded2000
- HeadquartersManchester, United Kingdom
- Headcount101–250
- GTM typeB2B
- OfferingServices
What Medicines Evaluation Unit does
Medicines Evaluation Unit Ltd (MEU) is a UK-based contract research organization (CRO) founded around 2000 and headquartered in a purpose-built, 36-bed hospital-based research facility in Wythenshawe, Manchester, with a satellite unit (MEU Quays) opened in 2023 at Salford Quays. MEU specializes in early phase clinical trials, offering Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) trials, bioequivalence studies, pharmacodynamic assessments, and specialist patient cohort programs across respiratory, dermatology, cardiovascular, inflammatory, and diabetes therapeutic areas. The organization has conducted over 370 clinical trials involving more than 10,000 patients over its 20+ year history.
MEU's core technology stack centers on the proprietary I.C.A.R.U.S. clinical database and trial management system, which holds demographic and clinical records on over 45,000 volunteers and patients and enables protocol-specific feasibility analysis and rapid recruitment. Supporting capabilities include an MHRA Phase I accredited pharmacy with GMP Grade C aseptic assembly, an in-house Phase I research facility with cardiac/telemetry monitoring and an outpatient assessment suite, a specialized bronchoscopy suite, and an extensive pharmacodynamics capability spanning ECG, telemetry, EEG, lung function, and challenge models. MEU also leads UK expertise in propellant testing for low global warming potential (GWP) inhalers (HFA-152a and HFO-1234ze), building on its role in the original CFC-free inhaler transition.
MEU generates revenue by selling clinical research services to pharmaceutical and biotech sponsors under direct enterprise contracts, with a go-to-market built on enterprise field sales, MHRA Phase I accreditation (held continuously since July 2009 with a clean inspection record across seven inspections through March 2025), KOL engagement, and integration with the Manchester University NHS Foundation Trust, the University of Manchester, and the North West Lung Centre Charity. The company is privately held and operates as an IQVIA subsidiary, with sister company CRO-Solutions providing additional capacity at Salford Quays and a partner network of accredited Phase I units across England and Wales extending reach for niche patient populations and radiolabelled studies.
Medicines Evaluation Unit firmographics
Firmographics- Name
- Medicines Evaluation Unit
- Legal name
- Medicines Evaluation Unit Ltd
- Website
- https://meu.org.uk
- Company type
- Private
- Founded year
- 2000
- Operating status
- Operating
- Headcount range
- 101–250 employees
- Short description
- Medicines Evaluation Unit (MEU) is a UK-based, MHRA-accredited Phase I contract research organization (CRO) and IQVIA subsidiary specializing in early phase clinical trials across respiratory, dermatology, cardiovascular, inflammatory, and diabetes indications, operating a 36-bed facility in Manchester and a Salford Quays satellite.
- Ownership category
- akta.pro rank
Medicines Evaluation Unit industry classification
Industry- Product category
- Contract Research Organization (CRO) Services
- NAICS
- Scientific Research and Development Services (5417)
- SIC
- Services-Medical Laboratories (8071)
- akta.pro primary industry
- Clinical CROs (Phase I–IV) (HLAGAAAA)
- akta.pro secondary industry
- Central Laboratory & Clinical Trial Testing CROs (HLAGAAAE)
Keywords
Where Medicines Evaluation Unit is headquartered
LocationHeadquarters
- HQ city
- Manchester
- HQ country
- United Kingdom
- HQ region
- Europe
Offices2 records
Markets served
Medicines Evaluation Unit business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain
Revenue model
- Clinical Research Services (CRO): MEU operates as a contract research organization providing Phase I-IV clinical trial services to pharmaceutical and biotech companies. Revenue is generated through conducting clinical trials on behalf of clients, including SAD and MAD trials, bioequivalence studies, pharmacodynamic assessments, and patient cohort studies. Services include regulatory consultancy and clinical supply capabilities.
Go-to-market motion1 record
Distribution channels3 records
Marketing channels7 records
Medicines Evaluation Unit product offering
Product offeringCore offering
Medicines Evaluation Unit (MEU) is a UK-based contract research organization (CRO) specializing in early phase (Phase I) clinical trials for pharmaceutical and biotechnology companies. The company operates a 36-bed hospital-based research facility in Manchester, conducting SAD and MAD trials, bioequivalence studies, pharmacodynamic assessments, and patient cohort studies across therapeutic areas including respiratory, dermatology, cardiovascular, inflammatory, and diabetes. MEU also provides specialized propellant testing services for climate-friendly inhalers and runs an MHRA-accredited pharmacy.
Product overview
Medicines Evaluation Unit (MEU) is an IQVIA business and UK-leading Contract Research Organization (CRO) specializing in early phase clinical trials. The company operates from a state-of-the-art 36-bed hospital-based research facility in Manchester with a satellite unit at MEU Quays. Core offerings include I.C.A.R.U.S., MEU's proprietary clinical database and trial management system, which underpins recruitment and study management across multiple therapeutic areas. MEU provides Phase I clinical trial services with MHRA accreditation, spanning respiratory, dermatology, cardiovascular, inflammatory, and diabetes therapeutic areas, alongside specialized capabilities in bioequivalence studies, pharmacodynamics, pharmacy services, recruitment, research and development, and propellant testing for climate-friendly inhalers.
Differentiator
Problem solved
Functional benefit
Products and services
- Phase I Clinical Trials Early phase clinical trial services including Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) trials, with expertise in hybrid designs including patient cohorts. Serves pharmaceutical and biotech companies seeking single-site solutions for early phase programmes.
- Bioequivalence Studies Bioequivalence studies in both healthy subjects and patient populations, including single-dose and steady-state studies with fed-state expertise.
- Respiratory Clinical Trials Specialist respiratory clinical trials in Asthma, COPD, Cystic Fibrosis, and Allergy with over 300 studies conducted. Database includes over 4,500 asthmatics and nearly 2,000 COPD patients.
- Dermatology Clinical Trials Clinical trials for skin conditions including psoriasis, eczema, and urticaria with expertise in PD markers, skin biopsies, and assessments including EASI, PASI, BSA, PGA, and SCORAD.
- Cardiovascular Clinical Trials Clinical trials in cardiovascular conditions with database of over 2,500 patients. Focus areas include hypertension, high cholesterol, atrial fibrillation, and heart failure.
- Inflammatory Clinical Trials Clinical trials for inflammatory conditions including psoriasis, atopic dermatitis, and rheumatological/auto-immune diseases.
- Diabetes Clinical Trials Clinical trials for diabetes and metabolic/endocrine conditions with a database of over 700 diabetes patients for fast and responsive recruitment.
- Pharmacy Services MHRA accredited pharmacy with GMP Grade C aseptic suite, IMP storage capabilities at ambient, refrigerated and frozen temperatures, and experience in aseptic technique, complex packing, and capsule filling.
- Recruitment Services Volunteer and patient recruitment with I.C.A.R.U.S. database hosting over 45,000 volunteers and access to catchment area of 2.8 million patients through Greater Manchester Primary Care Network.
- Pharmacodynamics Pharmacodynamic assessments including ECG, telemetry, imaging, respiratory capabilities, and challenge models for clinical trial endpoints.
- Propellant Testing Testing services for climate-friendly inhalers and low global warming potential (GWP) propellants including HFA-152a and HFO-1234ze to support transition towards environmentally sustainable inhaled drug delivery.
- Research and Development Collaborative R&D with Manchester University NHS Foundation Trust including cell culture, immunoassays, immunohistochemistry, PCR, flow cytometry, and western blotting for biomarker development.
- MEU Quays Satellite clinical trial facility at Salford Quays with reception, 6 clinic rooms, and 8 beds for additional clinical trial capacity.
Quantifiable outcome
- Over 370 clinical trials completed with 10,000+ patients involved
- +3 more outcomes
Companies that use Medicines Evaluation Unit
Customer profileNamed customers2 records
Segments6 records
Ideal customer profiles3 records
Medicines Evaluation Unit technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
Medicines Evaluation Unit partnerships and signals
Strategic signalPartnerships
Ten partnerships are on record, tiered core and minor.
- BespakcoreStrategic partnership to accelerate clinical trials on climate-friendly inhalers. MEU brings clinical trial expertise and regulatory consultancy while Bespak provides clinical supply capabilities at its Holmes Chapel site for manufacturing pMDIs containing new low GWP propellants (HFA-152a and HFO-1234ze). The collaboration aims to fast-track time to clinic and increase throughput of low GWP pMDIs moving through clinical evaluation.
- EpiEndominorClinical trial partnership where MEU served as a clinical site for EpiEndo's Phase 2A clinical trial for EP395 in COPD patients. The study enrolled 61 adults across 6 clinics in UK and Germany.
- Upstream BiominorMEU provided one-site solution for Upstream Bio's clinical trial leads, including development of a complex flow cytometry assay for monitoring drug pharmacodynamics in allergic and inflammatory conditions trials.
- IQVIAcoreMEU is an IQVIA business, operating as part of the global IQVIA organization (NYSE:IQV), a leading global provider of clinical research services, commercial insights and healthcare intelligence.
- CRO-SolutionscoreSister company to Medicines Evaluation Unit Ltd located at Salford Quays. Offers single site solution for all clinical trial needs, providing integrated capacity alongside MEU.
- Greater Manchester Blood BikesminorMEU supports the local volunteer blood bike service which transports vital medical supplies including blood, plasma, platelets, samples, vaccines, and donor breast milk to hospitals and healthcare facilities. MEU has raised £12,565 for this charity.
- North West Lung Centre CharitycoreThe North West Lung Centre Charity is the major shareholder of MEU and has received over £10 million in donations from MEU. The charity funds independent academic research and patient care within the NHS, supporting lung cancer screening and treatment innovations.
- Manchester University NHS Foundation TrustcoreMEU works in collaboration with Manchester University NHS Foundation Trust, led by Professor Dave Singh (Head of Airway Pharmacology Group). Research includes cell culture, immunoassays, immunohistochemistry, PCR, flow cytometry and western blotting for biomarker development in early clinical trials.
- University of ManchestercoreAcademic partnership with University of Manchester including Professor Dave Singh as Professor of Respiratory Pharmacology. Multiple research collaborations and clinical academic positions supported through the North West Lung Centre Charity.
- TORCH (Thoracic Oncology Research Hub)coreUnique collaboration between physicians, surgeons, radiologists and pathologists at North West Lung Centre. Part of Cancer Research UK's Lung Cancer Centre of Excellence, involved in national studies and the Tracer X collaboration with University College London.
Scale indicators7 records
Recent moves7 records
Expansion highlights5 records
Medicines Evaluation Unit competitors and assessment
Company assessmentDirect peers
- Celerion: Global early-phase clinical research organization specializing in Phase I/IIa studies and bioanalytical services; directly comparable therapeutic-area focus and single-site Phase I delivery model.
- Quotient Sciences: UK-based early-phase CRO offering integrated Phase I clinical and manufacturing services with strong respiratory and hybrid SAD/MAD patient-cohort capabilities, directly comparable to MEU's single-site Phase I model.
- Richmond Pharmacology: London-based specialist Phase I clinical research unit running SAD/MAD and patient-cohort studies with strong academic and NHS ties; a direct UK competitor for early-phase respiratory and inflammation trials.
- Hammersmith Medicines Research: UK Phase I unit with extensive first-in-human experience across healthy volunteer and patient studies, including vaccine and respiratory trials; closely comparable in scale and operating model to MEU.
- Simbec Research: Wales-based early-phase CRO offering Phase I healthy volunteer and patient studies with particular strengths in respiratory and specialist pharmacodynamics; competes head-to-head with MEU for UK early-phase contracts.
Broad incumbents
- ICON plc: Global CRO with extensive early-phase and bioanalytical capacity post-PRA Health Sciences acquisition; broad incumbent that competes with MEU for large multi-arm respiratory and inflammation programs.
- Parexel International: Large global CRO offering Phase I–IV clinical development services; competes with MEU for enterprise respiratory and early-phase programs while providing multi-site, multi-geography scale MEU cannot match.
- PPD (Thermo Fisher Scientific): Global CRO within Thermo Fisher offering Phase I–IV clinical development and central lab services; competes for enterprise early-phase respiratory contracts as part of an integrated platform.
- Labcorp Drug Development (Covance): Global CRO with significant early-phase clinical pharmacology and central laboratory capabilities; broad incumbent offering integrated Phase I and bioanalytical services that overlap with MEU's offering.
- Syneos Health: Global biopharmaceutical solutions organization providing Phase I–IV clinical development services; competes for enterprise respiratory and inflammation early-phase work as a broad incumbent vendor.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat5 records
Key risks6 records
Key highlights7 records
Customer concentration
Medicines Evaluation Unit social profiles
Digital presenceMedicines Evaluation Unit compliance and trust
Trust signalCompliance8 records
Medicines Evaluation Unit financial estimates
Financial estimateRevenue estimate
Valuation estimate
Medicines Evaluation Unit leadership team
Management profileNumber of profiles
Profiles5 records
Medicines Evaluation Unit funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Medicines Evaluation Unit M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Medicines Evaluation Unit
What does Medicines Evaluation Unit do?
Medicines Evaluation Unit (MEU) is a UK-based contract research organization (CRO) specializing in early phase (Phase I) clinical trials for pharmaceutical and biotechnology companies. The company operates a 36-bed hospital-based research facility in Manchester, conducting SAD and MAD trials, bioequivalence studies, pharmacodynamic assessments, and patient cohort studies across therapeutic areas including respiratory, dermatology, cardiovascular, inflammatory, and diabetes. MEU also provides specialized propellant testing services for climate-friendly inhalers and runs an MHRA-accredited pharmacy.
Is Medicines Evaluation Unit a public or private company?
Medicines Evaluation Unit is a private company. It is classified as corporate owned and is currently operating.
When was Medicines Evaluation Unit founded?
Medicines Evaluation Unit was founded in 2000. It employs 101 to 250 people.
Where is Medicines Evaluation Unit based?
Medicines Evaluation Unit is headquartered in Manchester, United Kingdom, in the Europe region.
How does Medicines Evaluation Unit make money?
One revenue line is on record: clinical Research Services (CRO).
Who are Medicines Evaluation Unit's main competitors?
Direct peers on record are Celerion, Quotient Sciences, Richmond Pharmacology, Hammersmith Medicines Research and Simbec Research. Broad incumbents are ICON plc, Parexel International, PPD (Thermo Fisher Scientific), Labcorp Drug Development (Covance) and Syneos Health.
Does Medicines Evaluation Unit have an API?
No public API is recorded for Medicines Evaluation Unit.
What industry is Medicines Evaluation Unit in?
Medicines Evaluation Unit's product category is Contract Research Organization (CRO) Services. Its primary akta.pro industry code is HLAGAAAA, Clinical CROs (Phase I–IV), with a secondary code of HLAGAAAE, Central Laboratory & Clinical Trial Testing CROs. Its NAICS code is 5417 and its SIC code is 8071.