Courses

All Courses are practical and include case studies. Regulatory perspectives from FDA/MHRA/EMA are provided based on expert input. Computer based analyses also available. Collaborations with experts in regulatory and leading researchers in academia.

Basic Statistics Courses

Understanding Statistics in Medical Research (Basic)
Understanding Statistics in Medical Research (Advanced)
Understanding Health Economics for HTA and Re-imbursement
Understanding Clinical Trials
Statistical Analysis of Clinical Trial Data

Advanced Statistics Courses

Statistical Methods in Clinical Trials
Statistical Methods in Real World and Observational Studies
Statistical Methods for Health Technology Appraisal and Re-imbursement
Modelling Cancer Data for Health Economic Models
Health Economic Models (Partitioned Survival, Cohort, Decision Tree etc)
How to develop and implement a health economic model for HTA
HTA requirements for different countries
Adaptive Designs : Design and Analysis (including Platform and Umbrella Designs)
Early Phase Trial Design: Bayesian Dose Escalation
Statistical Methods for Real World and Observational Studies
Statistical Methods For Devices and Diagnostics

Statistics Courses for Health Technology Appraisal and Drug Licensing

How do regulatory statisticians from FDA/EMA and MHRA review your clinical trial dossier
How do reviewers from NICE and ERG review your HTA Dossier
Statistical Methods in Drug Licensing and HTA