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The understanding of all drugs being potential poisons is not new to anyone in the pharmaceutical industry. Even at therapeutic doses, some medications are not selective enough in their pharmacology and often interfere with surrounding organs and systems. Pharmacovigilance is that construct that allows for the monitoring of a new pharmaceutical substance or device once it has been released into the market.
When properly implemented, it should reveal adverse reactions and provide information over a timeline that helps prescribers make better decisions concerning the use of the given agent. This course exposes students to the origin of pharmacovigilance and the key players at the global and local levels.
In this course, we provide a synthesis of the topic through an interactive online experience. This material was built by a team of Regulatory Affairs Experts with a Qualification from Northeastern University, Boston, piloted by a Senior Member able to articulate theory with practice.
Lesson 1: Historical Perspectives of WHO Drug Safety Management
Lesson 2: Current Practices of Pharmacovigilance
Lesson 3: Partners in Pharmacovigilance
Lesson 4: Drug Regulation Under Pharmacovigilance
Lesson 5: Pharmacovigilance and International Health
Lesson 6: Future Challenges and Drug Safety Considerations