Course Overview

Drug safety monitoring and risk management are vitally important for medicinal product developers, licence holders and clinical investigators. In addition to their duty to protect public health, increasingly tight regulation and potentially massive payments to litigants provide strong incentives for pharmaceutical and biotechnology companies to ensure that they maintain efficient systems for drug safety / pharmacovigilance and that all staff are aware of the basic requirements. This course will provide them with an overview of the most important aspects of this discipline, both before and after marketing of products, especially as they apply in Europe and the USA.

Who will benefit from this module?

Entry-level staff, and those seeking a refresher, in drug safety / pharmacovigilance and clinical departments will find the course invaluable, as will clinical investigators and other healthcare professionals. Staff in other departments of pharmaceutical and biotechnology companies will benefit from taking the course to gain an appreciation of the basics of the subject.

Learning objectives

1. Explain, with examples, why drug safety monitoring / pharmacovigilance is necessary.
2. Describe ways in which drug safety / pharmacovigilance is regulated nationally and internationally, and identify international policy-making bodies.
3. Outline how drug safety / pharmacovigilance responsibilities are organised within pharmaceutical and biotechnology companies.
4. Sketch how a product safety database is compiled, how a product’s safety profile is assessed, and how safety information is included in documentation for regulatory authorities, healthcare professionals, and consumers.
5. Apply appropriate terms to describe different types of adverse effect.
6. Specify requirements to report adverse reactions to regulators. Outline requirements for safety data and for risk management plans in applications for marketing approval.