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

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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Von Willebrand Disease Trial – First Stage of Hemab Therapeutics’ Trial Completed and New Patients Invited to Enrol

April 2, 2025
Richmond has completed dosing the first cohort of patients in Velora Pioneer, a phase 1/2 clinical trial investigating Hemab...
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Events

Swiss Biotech Day 2025

5–6 May 2025
Richmond Pharmacology is pleased to confirm our participation at Swiss Biotech Day 2025
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