Clinical Trials
Pharmaceutical Supply
for Sponsors and CROs
Euro Biom is an MHRA WDA-licensed wholesale distributor sourcing Investigational Medicinal Products, comparator drugs, reference standards and ancillary trial supplies for pharmaceutical sponsors, contract research organisations and clinical research sites globally.
⚡ Same-day response to every brief · Mon-Fri 09:00-18:00 · WhatsApp us
comparators and ancillaries.
Euro Biom sources the medicinal products required across all phases of clinical research. From single-batch comparator orders for a Phase II study to ongoing IMP supply across a multi-country Phase III programme, we work with the precise specification, quantity and timeline you submit.
Our scope includes Investigational Medicinal Products under MHRA-authorised pathways, branded comparators and Reference Listed Drugs (RLDs) for active-control arms, reference standards for analytical work, and ancillary trial supplies such as rescue medications, standard-of-care drugs and supportive medications required by the protocol.
We do not act as the sponsor, manufacturer or contract packaging organisation. We are the licensed wholesale dealer that locates verified product, secures it, documents it to GDP standards and ships it to the trial site you nominate.
Research Institutions
Clinical trial supply is a small, specialised market. The buyers and protocol stakeholders we work with most.
The authorisations that
make trial supply defensible.
Clinical trial sourcing involves layered regulatory obligations. Euro Biom holds the wholesale licensing required and works within the trial-specific authorisations held by the sponsor or CRO.
MHRA Wholesale Dealer Authorisation
Euro Biom holds WDA(H) 59239, granted by the Medicines and Healthcare products Regulatory Agency on 17 March 2026. This authorisation covers procurement, supply and export of medicinal products including those used as IMPs and comparators. Publicly verifiable on the MHRA register.
UK Good Distribution Practice
All clinical trial product is handled to UK GDP guidelines. This includes qualified personnel, documented quality system, validated cold chain, calibrated temperature monitoring, deviation management and full chain-of-custody records from authorised supplier through to delivery at the trial site.
UK and EU Clinical Trial Regulation Alignment
Sponsors and CROs hold the Clinical Trial Authorisations and operate under MHRA frameworks, EU Clinical Trials Regulation 536/2014 and, where applicable, US FDA IND requirements. Our role is to source and supply within those frameworks, ensuring documentation supports sponsor regulatory submissions and inspections.
Manufacturing and Packaging Coordination
Where blinded supply, over-encapsulation, label translation or matched-placebo coordination is required, we work with MHRA MIA(IMP)-licensed packaging and manufacturing partners. Euro Biom remains the named wholesale supplier; the licensed manufacturer handles any physical reconfiguration of the product.
to Trial Site Delivery
A four-step process designed for the documentation, traceability and timing demands of regulated clinical research.
Major Research Categories
Comparator and IMP requirements arise across every therapeutic area. Euro Biom has supplied or quoted on trials in each of the following.
control across every tier.
Modern clinical trial portfolios increasingly involve biologics, cell therapies and gene therapies with strict temperature requirements. We coordinate validated cold-chain handling across the full range, with calibrated monitoring on every shipment.
Temperature deviations are flagged immediately. Any excursion outside the validated range is documented, escalated and product is quarantined pending sponsor review. No untested product reaches a trial site.
Learn more about cold-chain capability →Submit a Clinical Trial Sourcing Brief
Send us the protocol specification. We assess feasibility, identify sourcing routes and respond the same working day with options, indicative timelines and documentary evidence.
Common questions from sponsor supply leads, CRO sourcing managers and clinical research investigators.
Further reading for clinical trial supply leads, sponsors and CROs.