Strategic Scientific Guidance

DRMRC advises pharma, biotech, research centres, and agencies across discovery, trial design, and regulatory preparation—delivering evidence-based, globally informed decisions.

  • Biomedical material strategy & evaluation
  • Clinical trial design & protocol development
  • Regulatory & compliance advisory (GCP/ICH/EMA/FDA)
  • R&D planning, investment readiness & tech transfer
  • Supplier, laboratory & partner selection
Consultation & strategic planning illustration
High-level consultation backed by clinical and regulatory experience.

Our Consultation Services Cover

1 Biomedical Material Strategy & Evaluation
  • Selection aligned to therapeutic goals
  • Assessment of potency, safety, and commercial value
  • Regulatory classification guidance (extract, biologic, API)
  • Sourcing regions & supplier strategy
2 Clinical Trial Design & Protocol Development
  • Ethical, statistically robust study designs
  • Phasing, controls, endpoints, and efficacy metrics
  • Risk–benefit, sample size, and statistical plans
  • Alignment with GCP, ICH, EMA, FDA
3 Regulatory & Compliance Advisory
  • Global approval pathways & submissions (IND/CTA/NDA)
  • IRB/ethics communication & documentation
  • Audit, inspection, and legal risk mitigation
4 R&D Project Planning & Investment Readiness
  • Feasibility & due diligence on early-stage programs
  • Market & competitor analysis
  • White papers, grants, investor materials
  • Tech transfer & licensing strategies
5 Supplier, Laboratory & Partner Selection
  • Evaluate CROs, labs, and suppliers
  • Introductions to vetted global partners
  • Contracts, MTAs, and confidentiality frameworks

Who Can Benefit?

Biotech Startups Pharma Pipeline Teams Academic Labs Gov’t & Nonprofit Agencies Investors & Strategic Partners

Why DRMRC?

  • MD/PhD-led, multidisciplinary expertise
  • Global reach across trials, suppliers, and sourcing
  • Evidence-based, ethically grounded advice
  • End-to-end support from concept to commercialization
  • Confidential, independent perspective

Research & Project Experience

Biomedical research context
Consulting across translational research and clinical pipelines.
Clinical project execution
From design to deployment—focused on outcomes and compliance.

Let’s Shape the Future of Medicine—Together

Launching a first-in-human study, evaluating a novel compound, or preparing for submission? DRMRC provides the clarity to move faster—confidently and compliantly.

Request Consultation → Visit drmrc.co.uk
Scroll to Top