Module Objectives
This module covers the practical management of the development of a medicine from Phase I to IV using research techniques to optimise efficiency in the development process. It also teaches students how to critically review and evaluate statistical data and to leverage and use the information.
Intended Module Learning Outcomes
Participate in most tasks needed to successfully conduct a clinical trial
Evaluate the suitability of different research methodologies for different types of clinical trials
Implement and manage suitable quality systems
Prepare and participate in audits and inspections.