Extended Services: Expert Consultation for Biomedical Research & Clinical Trials

Advancing Medical Innovation Through Strategic Scientific Guidance

At DE ROTHSCHILD MEDICAL AND RESEARCH CENTRE (DRMRC), we proudly offer a high-level consultation service to support research institutions, pharmaceutical companies, government agencies, and biotech innovators in their medical research and drug development programs.

With a decade-long foundation in biomedical science, clinical trials, and material sourcing, DRMRC is positioned as a trusted advisor for organizations seeking expert guidance, scientific clarity, and regulatory preparedness in complex biomedical ventures.

Our consulting service is rooted in deep scientific expertise, regulatory understanding, and global experience, helping partners at every stage of the innovation pipeline—from discovery to post-trial deployment.

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Our Consultation Services Cover:

1. Biomedical Material Strategy & Evaluation

• Advisory on selecting viable bio-resources based on therapeutic goals
• Scientific assessment of material potency, safety, and commercial value
• Guidance on regulatory classification (e.g., natural extract, biologic, API)
• Recommendations for optimal sourcing regions and supplier engagement

2. Clinical Trial Design & Protocol Development

• Assistance in designing ethically sound, scientifically robust clinical trials
• Structuring of trial phases, control groups, endpoints, and efficacy metrics
• Risk-benefit analysis, sample size justification, and statistical plan formulation
• Support in aligning with GCP, ICH, EMA, and FDA expectations

3. Regulatory & Compliance Advisory

• Navigation of local and international approval pathways
• Document preparation and review for submissions (IND, CTA, NDA, etc.)
• Support with IRB/ethics board communication and documentation
• Risk mitigation planning for audits, inspections, and legal exposure

4. R&D Project Planning & Investment Readiness

• Feasibility studies and due diligence on early-stage research or compounds
• Market and competitor analysis for proposed biomedical solutions
• Technical support in drafting white papers, grant proposals, and investor materials
• Advisory on technology transfer and licensing strategies

5. Vendor, Laboratory & Partner Selection

• Evaluating contract research organizations (CROs), labs, and vendors
• Facilitating introductions to vetted global partners in sourcing and trial execution
• Consultation on partnership contracts, material transfer agreements (MTAs), and confidentiality frameworks

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Who Can Benefit From Our Consultation Services?

• Biotech startups and spin-offs entering clinical or regulatory phases
• Pharmaceutical firms expanding their pipeline or exploring new materials
• Academic and private research labs in need of trial design or IP guidance
• Government or nonprofit health agencies launching funded clinical research
• Investors and strategic partners requiring expert technical due diligence

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Why DRMRC?

• Multidisciplinary Expertise: Our team includes MDs, PhDs, regulatory analysts, and pharmaceutical strategists
• Global Reach: Decade-long experience with international trials, vendors, and material sourcing
• Science-Backed Advice: All consultation is evidence-based, data-driven, and ethically grounded
• End-to-End Support: We guide you from conceptual design through clinical execution and commercialization
• Confidential & Independent: Full client confidentiality and neutral third-party perspective

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Let’s Shape the Future of Medicine—Together

Whether you’re launching a first-in-human study, evaluating a novel bio-compound, or preparing for regulatory submission, DE ROTHSCHILD MEDICAL AND RESEARCH CENTRE is your scientific ally.

We bring clarity to complexity, helping you make smarter decisions, reduce delays, and unlock the full potential of your medical innovation.

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To request a consultation or proposal, contact us at:
Email: consulting@drmrc.co.uk
Website: www.drmrc.co.uk