Adaptive Phase I & II Trials

Rapid approval, flexible conduct, adaptive protocols in a MHRA accredited facility.

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Phase III Clinical Studies

Fast and efficient patient recruitment for Phase III clinical trials.

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TQT Studies

Cardiac safety assessments are built into every clinical study.

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Bridging Studies

Fast track your global marketing authorisations with our ethnic bridging studies.

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Patient Recruitment

Fast and efficient in-house team, specialising in patient recruitment.

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Data Management

Flexible, efficient and tailored to our clients’ needs.

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Gene Editing & Gene Silencing

Richmond Pharmacology is at the forefront of gene editing.

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Latest news

Richmond Pharmacology Announces Promotion of Dr Priscilla Ochuba to Associate Medical Director

August 1, 2025
Richmond Pharmacology is pleased to announce the promotion of Dr Priscilla Ochuba to Associate Medical Director, effective 1st August 2025.
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Red4Research Blog – Alan’s Story

June 24, 2025
#Red4Research is a global initiative that recognises the essential role of clinical research in improving treatment, outcomes, and the future of medicine.
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Events

JSCPT 2025

5th –6th December 2025
Richmond Pharmacology will attend JSCPT 2025 in Tokyo, represented by their leadership team. Topics include early-phase studies, bridging studies between Europe and Asia, gene and RNA-based therapy development, and cross-border collaboration.
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