Training courses & Webinars:
Vigilance

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

A Practical Guide to Producing and Maintaining the PSMF Training Course

A Practical Guide to Producing and Maintaining the PSMF

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)

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A Practical Guide to Writing Risk Management Plans (RMPs) Training Course

A Practical Guide to Writing Risk Management Plans (RMPs)

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)

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Advanced Pharmacovigilance Training Course

Advanced Pharmacovigilance

5-7 Jun 2024 - Online webinar
Also on: 18 Sep 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)

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Advanced Veterinary Pharmacovigilance Training Course

Advanced Veterinary Pharmacovigilance

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)

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An Essential Overview of Medical Information Training Course

An Essential Overview of Medical Information

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)

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An Essential Overview of Pharmacovigilance Training Course

An Essential Overview of Pharmacovigilance

9-10 Sep 2024 - Online webinar

A practical guide to understanding the role of pharmacovigilance.

Presented by Graeme Ladds (bio)

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Cosmetovigilance Training Course

Cosmetovigilance

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)

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European Post Marketing Pharmacovigilance - Including the EMA/PRAC Deliberations and Brexit Implications Training Course

European Post Marketing Pharmacovigilance - Including the EMA/PRAC Deliberations and Brexit Implications

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)

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Introduction to Veterinary Pharmacovigilance Training Course

Introduction to Veterinary Pharmacovigilance

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)

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Pharmacovigilance Aspects of Licensing Agreements Training Course

Pharmacovigilance Aspects of Licensing Agreements

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

Presented by Joanne Flitcroft (bio)
Graeme Ladds (bio)

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Pharmacovigilance for Drug Safety, Regulatory Affairs and PV Auditors - Broadening your Knowledge Training Course

Pharmacovigilance for Drug Safety, Regulatory Affairs and PV Auditors - Broadening your Knowledge

30 Sep-2 Oct 2024 - Online webinar

This course has been designed for those wishing to learn more than the basics of Pharmacovigilance, who want to expand their knowledge and explore what they would like to understand next in this complex area.

Presented by Graeme Ladds (bio)

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Pharmacovigilance QMS & Inspection Preparation Training Course

Pharmacovigilance QMS & Inspection Preparation

20-21 May 2024 - Online webinar
Also on: 26 Sep 2024

This course is designed to help understand pharmacovigilance quality management systems (QMS) and risk-based audits.

Presented by Graeme Ladds (bio)

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Post-Market Surveillance - Practical Application for Medical Devices and IVDs Training Course

Post-Market Surveillance - Practical Application for Medical Devices and IVDs

6 Jun 2024 - Online webinar
Also on: 10 Oct 2024

Understanding the regulatory requirements for successful post-market surveillance of medical devices and IVDs is increasingly important and practical application of the regulations is key to a successful PMS system.
This course will provide a clear understanding of the intention of the requirements, and discuss the responsibilities of the manufacturer, notified bodies and competent authorities.

Presented by Anne Jury (bio)
Karen Pearson (bio)

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Practical Requirements of the Arab Pharmacovigilance Guidelines Training Course

Practical Requirements of the Arab Pharmacovigilance Guidelines

13-14 Jun 2024 - Online webinar
Also on: 17 Oct 2024

Practical guidance on how to comply with the pharmacovigilance requirements in the Middle East

Presented by Graeme Ladds (bio)

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Signal Detection and Regulatory Expectations Training Course

Signal Detection and Regulatory Expectations

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)

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Understanding Pharmacovigilance Regulations in APAC Training Course

Understanding Pharmacovigilance Regulations in APAC

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

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Excellent speakers and very experienced.

Joanna Jakubowicz, Deputy QPPV, Ovelle

All of the speakers were absolutely great, the talks were very interesting, informative and on a high level.

Yulia Buberman, PVG , Kamada LTD

The content of the course was comprehensive and the speakers gave a good oral presentation.

Markus Wollenweber, Owner, Wollenweber GMP/GDP-Services

This was a very good course; interesting and relevant content, good presentation and very competent speakers.

Ellinor Eliasson, Senior Quality Consultant, Scandinavian Regulatory Services AB

Yes the trainer was very good! I think that we have received a lot of new information.

Styliani Katsarou, Quality Consultant, Scandinavian Regulatory Services

It was very enlightening. The speakers spoke very calmly and with good diction.

Vivian Stefani, PV analyst, Eurofarma Laboratórios

Excellent speakers, comprehensive explanation, clear understanding... Very much recommendable

Anežka Staňková, SDEA Manager, ZENTIVA

A good presentation with lot of examples. The speaker is well versed with the topic and pharmacovigilance practices.
All other non-signal questions were also answered. Appreciate that

Sanam Chandwani, Manager Aggregate reports, Accord Healthcare

It was a very good webinar and a great topic, as I have not seen this topic in webinars before.

Dorte Jensen, QPPV Deputy, 2care4 Generics ApS

The speakers were both excellent.

Nuria Cabello, PV Manager and QPPV, Farmaprojects SAU