Date: November 9 (1 day)
Price: 6900 SEK per participant
Place: Physically at Hälsingegatan 40 in Stockholm (limitation of 12 participants) or Digitally
Course language: English
Diploma: Certificate is awarded after completion of the course
This course provides an introduction to the essential principles and practices of PV, the science and activities related to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. Furthermore, the course gives a comprehensive understanding of drug safety, including regulatory guidelines and industry practices. Topics covered includes the history of PV, adverse event reporting, overview of risk management, signal detection and benefit-risk assessment, as well as the latest technologies and tools used in pharmacovigilance. In summary, this course gives a solid foundation in the field of PV, ensuring to contribute to the safety of drugs in the market.
The lecturer for the PV course is Nidhi Arora. As a seasoned PV trainer with 12 years of hands-on experience, she has a wealth of knowledge in end-to-end PV systems, including ICSR case management, regulatory reporting, and signal detection. With over a decade of experience, she has a proven track record in writing, reviewing, and approving aggregate reports, risk management plans, and performing literature searches. Her skills and extensive knowledge of PV make her a valuable asset in training professionals to understand and implement effective PV practices. She is confident in her ability to create and deliver training programs that will help professionals develop their skills and succeed in their PV roles.
