Our pharmacovigilance training courses have been designed for drug safety professionals and will offer practical advice on key topics and the latest regulatory developments in this increasingly important field.
Pharmacovigilance has undergone a rapid regulatory change in recent years and become one of the most demanding aspects of the pharmaceutical industry to both understand and comply with.
We also provide training in vigilance and adverse event management for medical devices and pharmacovigilance for veterinary medicinal products and cosmetics.
Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book
5 Aug 2024 - Online webinar
Also on: 10 Oct 2024
This course provides a practical guide to both producing and maintaining the PSMF to ensure compliance and has been fully revised to include the latest updates.
Presented by Graeme Ladds (bio)
1 Aug 2024 - Online webinar
Also on: 9 Oct 2024
Understand the relationship between RMPs and safety reviews; PBRERs/DSURs; licence submissions (CTD) and their maintenance.
Presented by Graeme Ladds (bio)
18-20 Sep 2024 - Online webinar
Also on: 9 Dec 2024
This course will be of maximum benefit to those drug safety professionals who are working both in the clinical and post-marketing safety arena including QA for auditing.
Presented by Graeme Ladds (bio)
2-3 Jul 2024 - Online webinar
Also on: 9 Oct 2024
Including the main requirements of Volume IXB, an update on the proposed EU Regulation (2019/6) on Veterinary Medicinal Products and the impact of Brexit
Presented by Declan O'Rourke (bio)
11 Jul 2024 - Online webinar
Also on: 29 Nov 2024
In one day understand the role of medical information, the legal requirements for a medical information service, clarify the guidelines for medical information and advertising, receive practical advice on Black Triangle products and additional monitoring
Presented by Graeme Ladds (bio)
9-10 Sep 2024 - Online webinar
A practical guide to understanding the role of pharmacovigilance.
Presented by Graeme Ladds (bio)
20-21 Jun 2024 - Online webinar
Also on: 14 Oct 2024
This course will provide a comprehensive overview of cosmetogivilance in Europe, the USA and the Rest of the World (ROW).
It will provide key guidance for manufacturers and distributors on how to comply with the regulatory requirements, and will be valuable for pharmaceutical and medical device companies looking to access the cosmetic market.
Presented by Graeme Ladds (bio)
15-17 Jul 2024 - Online webinar
Also on: 4 Nov 2024
This course provides a comprehensive overview of key post-market pharmacovigilance activities required as the foundation for further understanding of new EU legislation that was introduced in 2012 and has undergone over 20 updates in the last 10 years.
Presented by Graeme Ladds (bio)
26-27 Jun 2024 - Online webinar
Also on: 2 Oct 2024
A basic training course for those working on drug safety in the EU. This course has been designed to provide basic training and a good introduction to those concerned with veterinary pharmacovigilance.
*INCLUDES: Interactive workshop and discussion sessions*
Presented by Declan O'Rourke (bio)
10 Jul 2024 - Online webinar
Also on: 27 Nov 2024
This programme will be of interest to all personnel involved in business development and licensing agreements aspects of pharmacovigilance
30 Sep-2 Oct 2024 - Online webinar
This course has been designed for those wishing to expand their knowledge in pharmacovigilance and explore what they would like to understand next in this complex area.
Presented by Graeme Ladds (bio)
26-27 Sep 2024 - Online webinar
This course is designed to help understand pharmacovigilance quality management systems (QMS) and risk-based audits.
Presented by Graeme Ladds (bio)
10 Oct 2024 - Online webinar
In this practical, one-day course, learn the regulatory requirements needed for successful post-market surveillance of medical devices and IVDs.
1-2 Jul 2024 - Online webinar
Also on: 12 Nov 2024
This two-day programme will give you a comprehensive review of signal detection and regulatory expectations including the new updated Signal Module IX and Eudravigilance quantitative signal requirement
Presented by Graeme Ladds (bio)
8-9 Jul 2024 - Online webinar
Also on: 8 Oct 2024
Pharmacovigilance regulations in Asia are dynamic and fast-changing. As the Asia-Pacific region becomes increasingly important for pharmaceutical companies, it's vital to ensure compliance and safety by staying informed of the latest regulatory developments.
Presented by
Param Dayal (bio)
and 4 more leading experts