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Consultancy & Scientific Advice for Drug Licensing & Re-imbursement

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Our Expertise

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  • Consultancy & Advice for Clinical Development Plans​

  • Evaluation of Briefing Documents​

  • Protocol Development Services​

  • Responding to Regulatory Agency Questions (e.g. FDA, MHRA, EMA)

R-S-S uses its network of clinical and medical experts to support clients on every step of their journey.

We offer consultancy to the biopharma industry and conduct continuous assessments on the ever-changing regulatory requirements in industry.

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Clinical Studies Design/Protocol Assistance

Our team provides comprehensive guidance in designing clinical studies, ensuring that they are scientifically robust, ethically sound, and regulatory compliant. We assist in protocol development, study design optimization, and endpoint determination to maximize the efficiency and success of your clinical trials.

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