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:
- Protocol and CRF Development
- Randomisation schedules
- Sample size calculations
- Statistical consultancy
- Statistical analysis
- Analysis, tables, figures and listings programming
- Statistical reporting
- Input into the integrated clinical/statistical reports