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

19 Jan 2024 - Online webinar
Also on: 24 Apr 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)

18 Jan 2024 - Online webinar
Also on: 16 Apr 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

11-15 Dec 2023 - Online webinar
Also on: 20 Mar 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

22-25 Jan 2024 - Online webinar
Also on: 16 Apr 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

15 Mar 2024 - Online webinar
Also on: 11 Jul 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

29 Jan 2024 - Online webinar
Also on: 16 May 2024

A practical guide to understanding the role of pharmacovigilance.

Presented by Graeme Ladds (bio)

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Artificial Intelligence and Machine Learning Powered Signal Management Training Course

Artificial Intelligence and Machine Learning Powered Signal Management

24 Jan 2024 - Online webinar
Also on: 15 May 2024

This course will prepare you to navigate the multiverse of Artificial Intelligence (AI), Machine Learning (ML) and Deep Learning from a drug safety perspective with an easily understandable and practical approach.

Presented by Sanjeev Srivastav (bio)

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Cosmetovigilance Training Course

Cosmetovigilance

5-6 Feb 2024 - Online webinar
Also on: 20 Jun 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

4-8 Mar 2024 - Online webinar
Also on: 15 Jul 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

5-8 Feb 2024 - Online webinar
Also on: 27 Jun 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 Training Course

Pharmacovigilance

31 Jan-2 Feb 2024 - Online webinar
Also on: 12 Jun 2024

Understanding PhV today – a basic training course on the principles and practice of global PhV for those working in drug safety.

Presented by Glyn Belcher (bio)
and 4 more leading experts

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Pharmacovigilance Aspects of Licensing Agreements Training Course

Pharmacovigilance Aspects of Licensing Agreements

29-30 Nov 2023 - Online webinar
Also on: 1 Mar 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

31 Jan-2 Feb 2024 - Online webinar
Also on: 8 May 2024

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

22-25 Jan 2024 - Online webinar
Also on: 20 May 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

14 Feb 2024 - Online webinar
Also on: 6 Jun 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 Feb 2024 - Online webinar
Also on: 13 Jun 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

18-19 Mar 2024 - Online webinar
Also on: 1 Jul 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

23-24 Jan 2024 - Online webinar
Also on: 23 Apr 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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In-house training

We can provide any of our courses on an in-house basis - at your location or online, with a programme and presenters tailored to your exact requirements. If you require training for multiple staff members, contact us to see how we can work with you.

Previous attendees said...

“Every item, but especially the topics of signal management & audits and inspections. I am grateful for the advise giving on how to approach audits/inspections.”

Charlotte Lindorf Eriksen, Head of Pharmacovigilance, QPPV, Billev Pharma ApS

“Excellent and engaging content using some 'real life' examples which offered context for greater insight, delivered by an experienced presenter who was able to provide additional depth when further questions were asked.
I thoroughly enjoyed it thank you!”

Claire Francis, LRRP and Regulatory Affairs Officer, Vetoquinol UK Ltd

“Specific, accurate and useful.”

Valdas Liukaitis, , SMCA of Lithuania

“Excellent, his experience and extensive knowledge are evident. It's been a pleasure to learn from him. I really liked the presentation and the speaker. Clear ideas, all the topics covered, and practical exercises to put the theory into practice.”

Eva Sanz Castel, GSM QA AUDITOR, Lab Esteve

“I really enjoyed the course and took a lot out of it. The real life examples were really helpful. ”

Joana Pereira, Senior RA Manager, Cycle Pharmaceuticals Ltd

“Practical knowledge of situations in Industry and the slides contained enough information to obtain a good understanding of an area that is complicated. the webinar was excellent, the speaker was very familiar with the most recent legislation ”

Martina Lee, Regulatory Affairs Specialist, NorthStar

“I refreshed my knowledge of Pharmacovigilance and learnt about changes in the industry. Excellent speaker, delivered in a clear and professional manner making it easy to follow and understand. Graeme came across in a relaxed manner, making the course more engaging.”

Nicky Wightman, Pharmacovigilance Support, Boots Pharmaceuticals

“I am very happy to have been on this course. It was very beneficial to my work.”

Ciara Cousins, Clinical Vet and Veterinary Advisor, Norbrook

“Overall, the speaker was very competent and added a lot of real-world examples and thus enabled better understanding of the theory/regulatory requirements presented. He is an excellent trainer.”

Daniela Bausewein, Associate Director Clinical Safety Management, BioNTech SE

“Was so good”

Hammad A Al Dali, Expert in Pharmacovigilance System Inspection, Saudi Food & Drugs Authority