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

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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Richmond Appoints Lisa Campbell as Director of Regulatory Strategy

April 23, 2025
Richmond Pharmacology is pleased to announce the appointment of Lisa Campbell as Director of Regulatory Strategy
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Events

BIO International Convention 2025

16-19 June 2025
Richmond Pharmacology will be attending the BIO International Convention 2025 in Boston, connecting with biotech innovators at Booth 765.
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