World-class
Scientific Advisory

Work with Richmond Pharmacology and trust your experience will be personal and truly strategic.

What makes us special?

Work with Richmond Pharmacology and trust your experience will be personal and truly strategic.

What makes us special?

Richmond Pharmacology delivers clinical excellence from design to delivery. Our long-term working relationships with our international client-base has led to the completion of over 500 Early Phase Studies.

We provide a personal service. Our founders are influential clinical research experts and lead each clinical trial. Our team of senior drug development experts are also on hand to ensure the quality, integrity, and accuracy of your study. We are reputed for our customer-centric project management, our flexible approach, and the superior quality of the studies. As a sponsor, you will have high-level engagement and meaningful peer to peer conversations.

Accredited by the MHRA, we guarantee that our trials adhere to the highest clinical, ethical and safety standards and our processes are auditable.

Our efficient and adaptive approach leads to faster development times, accelerating the time to market from first in human trials to proof of concept in under nine months. Adding value by integrating ethnic comparison elements and intensive cardiac assessments.


The clinical unit is in the heart of London with easy access to mainline train stations and airports, making it the ideal location to attract research volunteers.

Richmond Pharmacology’s volunteer database exceeds 250,000 individuals from a broad demographic spectrum and a wide variety of patient panels across rare to more common diseases. The database grows by 1000 to 2000 volunteers each month with a typical 70/30 split between healthy volunteers and patients.

Latest news

Upcoming Event

On Helix, Transforming new medicine discovery

13-14 July 2020
Richmond Pharmacology will be showcasing a presentation on Adaptive Early Phase Clinical Trials as part of the ON HELIX digital event.
View event

COVID-19 – External Monitoring Guidelines

July 1, 2020
Richmond Pharmacology is constantly assessing health and safety risks posed by COVID-19 and is regularly reviewing Public Health England guidance.
Read more

First transdermal patch to treat schizophrenia hits market

March 18, 2020
The US Food and Drug Administration (FDA) has officially approved a transdermal patch to treat schizophrenia developed by Hisamitsu Pharmaceutical Co following successful
Read more

Statement: COVID-19

March 23, 2020
Richmond Pharmacology are continuously risk-assessing our activity in relation to the COVID-19 crisis and we are evaluating what activity can continue, what precautions need to be put in place and what needs to be suspended.
Read more