This module is designed for students with a particular interest or need to understand in detail the principles and practices required to collect high quality clinical trial data, to review and prepare clinical trial data for analysis in compliance with regulatory requirements and Good Clinical Practice (GCP).It is an option for all the students on PG Diploma/MSc Clinical Trials, PG Diploma/MSc Global Health Policy programmes.
15 [150 hours]
Formal assessment of the module will be by an assessed assignment (20%) and by a 2hr 15 unseen written examination (80%).
If you fail the module overall, you are allowed one further attempt at the failed element (examination and/or assignment).
For full information regarding this module please see the module specification.