Focused and dedicated
Our speciality is in making complex tasks simple. As well as being project-based, our statisticians are frequently on call to give advice on study design.
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A dedicated team
Clinical development programmes have dedicated teams of statisticians and programmers, able to respond quickly to changes in priorities.

Wide experience
Our statisticians and programmers have experience in a wide range of therapeutic areas and trial stages, contributing to some 70-80 studies per year.

Statistics

Working on a project team basis, our statisticians see each study through from protocol and CRF design to statistical report. With backgrounds in industry and academia our statistical team has extensive experience in all phases of clinical trials and many therapeutic areas.

We've a group concentrating on the special demands of oncology studies, and another working on early phase trials.

We operate a peer-review by dual independent programming of critical endpoint analysis, and all output is subjected to quality assurance review. Our program code is fully documented during development, passing through a formal validation procedure. The programs may be supplied with the statistical output and report, if required by our Sponsor.


Syne qua non | data management | electronic data capture | statistics
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Syne qua non Ltd
Navire House · Mere Street
Diss · Norfolk · IP22 4AG · UK
Tel   +44 (0) 1379 644449
Fax  +44 (0) 1379 644445

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