Clinical Research Biometrics

Aside from implementing successful tracking, and monitoring processes we can also provide specialist consultancy in the study design and data collection processes.

Our services include CRF design, data tracking, data entry, validation and study design as well as statistical support (sample size calculations, power calculations and randomisation schedules), analysis plans, table and listings generation and statistical analysis.

Our experience shows us that keeping a clinical trial on track depends on understanding the clinical research data management issues as they arise. At PRN the whole team is involved in review of the annotated CRF, therefore our Clinical Research Associates can follow the significance of the data points and their interpretation – leading to the collection of more meaningful data.