News release

Date: 16th September 2008

t+ Clinical’s mPRO Solution Shortlisted for Good Clinical Practice Journal Awards

Innovative Data Capture Solution For Pharmaceutical Customers Recognised in “Best Technological Development in Clinical Trials” Category

Oxford, United Kingdom, September 16th 2008 – t+ Clinical, the leading provider of mobile phone-based data capture solutions for late-stage clinical trials, today announces that its mPRO (mobile patient recorded outcomes) solution has been shortlisted for the Good Clinical Practice Journal (GCPj) Awards 2008. t+ Clinical is named as a finalist in the “Best technological development in clinical trials” category, which recognises the best advances in supporting clinical trial management. The winners of the GCPj awards will be announced at a gala dinner in London on 22nd October 2008.

The t+ Clinical mPRO solution runs over the world’s largest data infrastructure, operates on mobile phones in every geography, and delivers familiar, high compliance technology to study subjects worldwide. Using a unique yet practical method of gathering electronic patient recorded data through mobile phones, t+ Clinical is able to offer fast rollout within days of a finalised study, combined with real-time analysis of primary outcomes.

The annual Good Clinical Practice Journal Awards are designed to recognise the remarkable achievements of individuals and organisations working in the clinical trial industry. “Outstanding…Exemplary…Impressive” are just some of the comments given by the judges about this year’s GCPj entries, proving once again that the clinical trials sector is buzzing with innovation and a continued commitment to improving trial processes.


About t+ Clinical (
t+ Clinical was established in 2007 as a subsidiary to t+ Medical Holdings, to offer data capture solutions to pharmaceutical customers for late stage clinical trials. The vision of t+ Clinical is to enable the drug discovery process to move as quickly and accurately as possible through mobile phone based, late stage clinical trials. By ensuring that every stage of data collection and analysis is as efficient as possible, high standard results are delivered in the shortest time.

For further information please e mail info[at]tplusclinical[dot]com or call
Anna Griffiths +44 (0) 1235 432050

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