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

Five Years Since a World-First CRISPR Breakthrough at Richmond Pharmacology

December 8, 2025
In November 2020, Richmond Pharmacology made medical history when a patient received the first-ever systemically delivered CRISPR therapy, using lipid nanoparticles to edit genes directly inside the human body.
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Events

JSCPT 2025

5 – 6 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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