Regulation of pharmaceuticals is controlled by standards, guidelines and legal frameworks. The interactions among these and the stakeholders – industry, regulatory authorities, healthcare professionals and patients – are required for effective governance for safe, quality and efficacious medicines and timely access for patients. This fundamental module provides the understanding of the contribution of the various stakeholders, functions and guidelines that shape the regulatory environment and impact the healthcare management scene. The concept of product lifecycle will be also be explored among other contemporary regulatory approaches.
Course Fee: SGD$3,611.25
Due to the limited availability of seats, early registration is strongly recommended.
Click here for a step by step guide on how to register.
07 Sep 2020 @ 09:00 - 11 Sep 2020 @ 18:00