Statistics Statistics

Richmond statisticians are involved in all aspects of a data management project from protocol and CRF design to statistical reporting. Richmond Pharmacology’s statisticians have academic backgrounds with vast industry experience in all phases of clinical trials across numerous therapeutic areas.

Pharmacokinetics, bioequivalence and Thorough QT, (TQT), are areas of specialised skill and expertise for Richmond Pharmacology’s statisticians.

We operate a peer-review by dual independent programming of critical endpoint analysis, and all output is subjected to quality assurance review.

We provide the following statistics services:

Case studies

The thorough approach to QTc studies ("Your perfect partner for conducting definitive thorough QT studies, all under one roof")

Timelines, Tight Timelines and Even Tighter Timelines in a Phase I Environment (We know we can help your business. We always rise to the challenge)