Module I – Overview of Clinical Research

Module II – Pharmacology & BA be studies

Module III – Biostatistics

Module IV – Regulations and Guidelines

Module V – Design of Trials

Module VI – The Role of the Study Subject

Module VII – Ethics committee

Module VIII – Adverse Event Reporting

Module IX – Clinical Data Management

Module X – Audit & Monitoring

Module XI –  Investigational Drug Management

Module XII – Business Communication