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Our mission is to ensure the generation of accurate and precise findings.

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OUR SERVICES

Coordinating Scientific Researches That Promotes Development of Life Saving Medications

Biomedical Sourcing

Rare & potent materials for drug development

Clinical Research

Protocol design to post-trial reporting

Inspection Services

Third-party verification for materials and trials

Scientific Advisory

R&D strategy, compliance, and scale-up

Medical Sponsorships

Supporting promising projects globally

ABOUT US

Trusted Globally. Rooted in Science.

Founded in 2012 in London, UK, DE ROTHSCHILD MEDICAL AND RESEARCH CENTRE (DRMRC)

DRMRC is a research-led, procurement-focused organization specializing in the global supply of clinical-grade biomaterials and collaboration on medical trials and drug development.

Powering Health Solutions in 40+ Countries

30,000

Registered Clinical Volunteers

92

Million+ Pound Invested in Global Research

290

Million+ Pound Raised in Sponsorships

200

Verified Procurement Agents & Vendors

Who We Serve

Our Clients & Collaborators

From Big Pharma to biotech startups, DRMRC supports
  • • Pharmaceutical manufacturers
  • • Clinical trial sponsors
  • • Biomedical innovators
  • • Health ministries & NGOs
  • • Academic and institutional labs
Join Our Network

Whether You Are A

Supplier/Vendor

Apply to join our sourcing network

Sponsor/Donor

Support critical health research

Research Partner

Collaborate on trials and studies

Client/Buyer

Procure certified biomaterials with confidence

TESTIMONIAL

Quotes from industry clients or sponsors

DRMRC has been a game-changer for our lab. Their consistent supply of high-quality biomedical materials has accelerated our research timelines significantly.

Dr. Emily Harper
Principal Investigator, Genova Research Labs

We rely on DRMRC for critical biomaterials. Their global sourcing capability and professionalism are unmatched in the industry.

Dr. Miguel Alvarez
Head of R&D, NovaPharm Solutions

DRMRC understands what research teams need—speed, precision, and compliance. Highly recommended for any biomedical institution.

Dr. James Osei
Director of Clinical Trials, Medivance Global

Contact Research Team