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Ethically Approved Phase I Clinical Trials

The FIRST Clinical Research Organisation to conduct a Phase I trial in healthy young people aged 14-17! On the 12th February 2009 Richmond Pharmacology became the first CRO in Europe to gain ethics approval to conduct a Phase I healthy volunteer trial in healthy young females aged 14-17. Richmond Pharmacology is a clinical research specialist [...]

The FIRST Clinical Research Organisation to conduct a Phase I trial in healthy young people aged 14-17!

On the 12th February 2009 Richmond Pharmacology became the first CRO in Europe to gain ethics approval to conduct a Phase I healthy volunteer trial in healthy young females aged 14-17.

Richmond Pharmacology is a clinical research specialist

This landmark decision by Great Ormond Street Ethics Committee to allow this study to be conducted paves the way for future studies of this age group.

A great achievement for Richmond Pharmacology was the recruitment of the first healthy young volunteers just sixteen days after gaining ethics approval on 28 Feb 2009.

The study being conducted by Richmond Pharmacology aims to determine the effect a study drug, (a new oral contraceptive pill), has on the body and if there is a difference in what happens to the drug in females aged 18-50 compared to females aged 14-17.

The study itself is a usual characteristic of many Phase 1 clinical trials of these compounds, however it is the population being included that makes this a pivotal study.

The UK has been known to conduct top class clinical trials and studies for all phases   In recent years some trials that would typically be conducted in the UK have moved offshore to Eastern Europe and the Sub Continent. However the approval of this study marks a substantial shift in thinking and attitude towards clinical trial conduct in the UK and Richmond Pharmacology are proud to be at the centre of this pioneering move to once again make the UK THE place to conduct more specialised clinical research

In addition to providing high quality full service clinical studies, Richmond Pharmacology now has the proven ability to conduct a wide variety of studies complicated in their design and population required.

Richmond Pharmacology’s founding Directors are still at the heart of the company. Their hands on approach coupled with a dedicated and highly skilled staff ensure we are able to meet the challenges set by sponsors.

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