Clinical Trials - A Practical Guide to Design, Analysis, and Reporting by Duolao Wang, (PhD) and Ameet Bakhai (MBBS, MRCP) is the result of a unique collaboration between two experts in the exciting fields of medicine & science. The publication seamlessly integrates important contributions from leading clinicians in the research field, including Richmond Pharmacology's own Dr Radivoj Arezina, MD MSc, Research Director, and Dr Ulrike Lorch, MD, FRCA, MFPM, Medical Director.For more information please click on the following link:

Cover of Clinical Trials book featuring a cartoon doctor

If you wish to purchase the book it can be ordered directly from the publisher Remedica (www.remedica.com) or Amazon (http://www.amazon.com/Clinical-Trials-Practical-Analysis-Reporting/dp/1901346722)

Latest news

Futureproofing early phase clinical research for the next generation of investigators.

March 20, 2023
Richmond Pharmacology’s experienced Principal investigators and Co-investigators recently gave expert feedback on the ICH M11 (CeSHarP) protocol template.
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Director of Operations, Keith Berelowitz, has been appointed as the Research Ethics Committee Chair for the Health Research Authority.

January 19, 2023
Keith Berelowitz will be responsible for ensuring that all ethical possibilities are explored in relation to new research.
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Events

13th International Workshop on Regulatory Requirements and Current Scientific Aspects on the Preclinical and Clinical Investigation of Drug-Drug Interactions

Sunday, June 4th to Tuesday June 6th 2023
Exchange research-based knowledge on drug-drug interactions (DDIs) among all interested stakeholders from pharmaceutical industry, regulatory authorities, academic and health care delivery backgrounds and perspectives.
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