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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Regulatory Strategy Services

Strategic guidance for faster global regulatory approvals.

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Pharmacovigilance

Patient safety through expert adverse event monitoring

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Latest news

Richmond Pharmacology Appoints Dr Daniel Chapple as Commercial Director

July 13, 2026
Richmond Pharmacology, the London-based contract research organisation and global leader in early phase clinical trials, announces the appointment of Dr Daniel Chapple PhD FCIM as Commercial Director.
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Upcoming Event

ESC Congress 2026

28 - 31 August 2026
Richmond Pharmacology is pleased to attend the ESC Congress 2026 in Munich, Germany, on 28 - 31 August 2026.
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