Low data variability

Our core ECG laboratory provides a centralised system for all our studies. High precision ECG acquisition in our clinic provides meaningful ECG analysis with a smaller sample size, making us the ideal choice for the integration of cardiac safety in FIH and MAD studies.

We are a leading publisher in cardiology and have publicly accessible credentials. We are proud of our integrity, our professional growth and experience in this field.

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Exceptional ECG generation

We undertake and analyse several cardiological assessments using state-of-the-art equipment to understand and explain abnormal ECG data obtained during a clinical study of a new chemical entity.

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Experts in cardiac safety

Richmond Pharmacology’s Core ECG Laboratory team are based within St George’s Hospital Medical School, London and are made up of highly experienced cardiologists headed by Professor John Camm, a key opinion leader in TQT Trials.

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Our range of services cover phases I, II and III ECG safety studies for cardiovascular and non-cardiovascular compounds.

Many "normal" healthy volunteers will have abnormal ECGs or have abnormal ECGs which they are aware of. These abnormal ECGs may have a big impact on the development of a new chemical entity if the data obtained is not scrutinised properly at an early stage.

Early signal detection and full follow up by Richmond Pharmacology's cardiology team is essential to ensure that the digital ECG data obtained from an early phase trial is analysed and reported appropriately. Richmond Pharmacology has the capacity to undertake and subsequently analyse several cardiological assessments to understand and explain abnormal ECG data obtained during a clinical study of a new chemical entity.

Analysis services include rest and exercise ECG analysis, detailed digital QT analysis, entry criteria validation, cardiac event classification and Holter provision, analysis and review. The assessments are performed using Richmond's bespoke and integrated MUSE setup.

We ensure rapid and reliable digital ECG data is obtained to support the “go” or “no-go” decisions during your early phase trial.

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Latest news

Samarjit Singh promoted to New Director of Clinical Operations

August 30, 2022
Richmond Pharmacology is delighted to announce the promotion of Samarjit Singh into the position of Director of Clinical Operations.
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Transforming clinical trials to accelerate drug development – Keith Berelowitz

August 23, 2022
Dr Keith Berelowitz, Richmond Pharmacology’s Director of Operations, wrote recently for Pharmaceutical Market Europe where he outlined how innovations in the design and delivery of clinical trials are speeding up the discovery of new therapies for the benefit of patients, sponsors and health systems.
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Events

The Future of Healthcare - March 2022

13:30 – 16:00, 22nd March 2022
Discover the intricacies of assessing abnormal liver functions in clinical trial volunteers and gain insights from the latest drug development trials using RNAi therapeutics.
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