2022 GMS5108 Clinical Studies and Evaluation of Health Products (Conducted Remotely)

The effective regulation of pharmaceuticals for safety and efficacy depends on the availability, understanding and appropriate implementation of relevant guidelines and the processes designed to ensure quality in decision-making. The requirements are frequently different from traditional clinical trials and specific to regulatory affairs. This four-credit module provides the understanding for the unique requirements of clinical trials and clinical data meant to support regulatory evaluation and approvals.

Due to the limited availability of seats, early registration is strongly recommended.


Date and Time

17 Jan 2022 @ 08:30 - 21 Jan 2022 @ 17:30