Our latest COVID-19 information/status - including self-paced online learning from our training partner Falconbury

Training & Courses:

Pharmacovigilance has undergone rapid regulatory change in recent years and become one of the most demanding aspects of the pharmaceutical industry to both understand and comply with. Our 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.


Our spring/summer 2020 programme of London-based courses has been cancelled due to the COVID-19 outbreak. We are taking bookings for our Autumn events, but we are also working to deliver courses and content online. Please contact us if you are interested in an on-site or online version of any of our courses, tailored to your company's needs.

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.

Understand the relationship between RMPs and safety reviews; PBRERs/DSURs; licence submissions (CTD) and their maintenance.

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.

Advanced Pharmacovigilance

23-25 Sep 2020

Also on: 17 Mar 2021

A practical guide to understanding the role of pharmacovigilance.

An Essential Overview of Pharmacovigilance

5 Oct 2020

Also on: 26 Apr 2021

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


7-9 Dec 2020

Also on: 21 Jun 2021

This course will provide you with practical advice on preparing an effective audit report to ensure your readers understand the findings and the key messages you are trying to convey. Examples of common issues and pitfalls will be discussed to enable you to improve your audit writing skills.

We can customise this course to meet your requirements.

This programme will be of interest to all personnel involved in business development and licensing agreements aspects of pharmacovigilance

Pharmacovigilance Aspects of Licensing Agreements

9 Oct 2020

Also on: 15 Apr 2021

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

Pharmacovigilance QMS & Inspection Preparation

19-20 Nov 2020

Also on: 13 May 2021

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

Signal Detection and Regulatory Expectations

2-3 Nov 2020

Also on: 3 May 2021

Graeme was an extremely knowledgeable source who focused on imparting the most important information for us to understand the RMP writing process. I was looking to gain a better understanding of preparing RMPs in accordance with legislation and I believe that Graeme did an excellent job in providing this.

Rex Alexander, Pharmacovigilance Compliance Manager - EUPV, APL Swift Services (Malta) Ltd

The speaker is confident and clearly knows the subject well.

Christopher Harper, Pharmacovigilance and Medical Information Manager, Blue Earth Diagnostics

Overall an excellent course – it flowed very well and the examples that were provided throughout were helpful.

Chrissa Cooper , Associate Director QPPV Office & PV Alliances , Norgine Ltd

Excellent throughout. Graeme was very knowledgeable and engaging and the content was varied and at a good level.

Yasmy Kumar, Pharmacovigilance Manager , Red Line Pharmacovigilance

I found the course worthwhile. The presenter was easy to follow and gave practical examples which I found useful.

Laura Maginley, Manager, EU Regulatory Sciences, Biogen

Very good course that gave an overall understanding of the RMP and its purpose, presented by a very good communicator with many years of experience.

Tina Maria Greve, Drug Safety Advisor, ALK-Abello A/S

I loved the course and it was amazing to be taught by people who are very experienced in the topics and be able to get their insights and hear their experiences.

Tina Tayebi, Pharmacovigilance Associate, Diamond Pharma Services

I was really happy with this course which was complete and well presented. The speaker really knew his subject and kept the course alive with personal examples which was really entertaining. The course gave me some valuable ideas that I could implement in our qualitative signal detection.

Caroline Riaud, Pharmacovigilance Associate, Ceva Santé Animale

Very interesting course with a good speaker. I particularly liked the global view of pharmacovigilance and its impact on signal management.

Chloé Dubarry, Pharmacovigilance Associate, Recordati Rare Diseases

Comprehensive content, understandable presentations and a speaker with extensive experience.

Anne Kjøde, Medical Advisor/ QPPV, Karo Pharma AS