Training courses & Webinars:
Industry

 

Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book

Animal Health

Next events:

  • 17-18 Jun 2025 Advanced Veterinary Pharmacovigilance
  • 3-4 Jul 2025 Introduction to Veterinary Pharmacovigilance

See all 8 courses

Biopharma

Next events:

  • 11 Jul 2025 US FDA - Understanding Key Factors When Working with the FDA
  • 26 Nov 2025 US FDA - Understanding Key Factors When Working with the FDA

See all 2 courses

Cosmetics

Next events:

  • 19-20 Jun 2025 Cosmetovigilance
  • 13-14 Oct 2025 Cosmetovigilance

See all 2 courses

Medical Devices

Next events:

  • 22 May 2025 The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR
  • 16-17 Jun 2025 Medical Device Regulations in the Middle East and North Africa

See all 44 courses

Pharmaceutical

Next events:

  • 20-21 May 2025 Process Validation with Qualification
  • 21-22 May 2025 Drafting Commercial Contracts for the Pharmaceutical Industry

See all 114 courses

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...

“Very competent.”

Jesper Bergwik, Regulatory Affairs Associate, Bioglan AB

“Was very useful. I feel I accomplished further knowledge about the implementation of MDR and IVDR and also what is on the horizon in terms of the UK regulations from the course. The content of update on IVDR was great as it was directly related to my work. I also enjoyed learning more about the history of the regulations/legislative process and gained some useful background knowledge on combination products. ”

Liz Gillman, Clinical Compliance Project Lead, LifeScan Scotland

“EXCELLENT - worth the time and money. I hoped to gain additional knowledge in Pharmacovigilance/show me areas where I may be lacking. I did not want the training to be a waste of time out of the office...[it was] definitely not — I would highly recommend
the speaker and the course. 5/5 overall.”

Nicky Höll, Pharmacovigilance Manager, Eurolab (Pty) Ltd

“Overall, 5* - Excellent. I learnt a lot of things in detail. Now happily I can implement those with my current job. All the sessions very helpful for me. Excellent speaker, explained very well and in detail for every question. ”

Vijaya Laxmi-Tunakala, QA Officer, Pharmacare Premium Ltd

“An excellent webinar, delivered by a very knowledgeable person in an impactful way by great use of analogies and first hand experiences that brought the learning to life. First experience and a very pleasant one.”

Lee Gittings, Country Manager, Biofrontera UK Ltd

“The speaker was excellent and shared a lot of interesting information regarding national registration in the CIS region. All in all, it was good and useful webinar.”

Marina Baum, CMC specialist, JGL d.d.

“Overall the course is well organized, contains relevant information and provides a good starting point for registration activities in the covered geographical area. I think if a person gets responsibility for regulation in EUEA, Russia, Ukraine, Kazakhstan and Belarus countries — this course is a great source of relevant information. ”

Elena Dolgodilina, Regulatory Affairs Manager, Geistlich

“The training materials were well prepared and of high quality. These will be an excellent reference when we want to start planning device registrations for US market. Overall, very happy with the content, speaker and presented materials.”

Veerle Leijnen, Senior RA Executive Manager, Nikkiso Belgium

“That was perfect, thank you! The presentation, content and presenter were very good. I hoped to get basic understanding of the FDA submission pathways and this is certainly achieved! Overall, I am very satisfied having followed the course.”

Elisabet Jamez, Biocompatibility Expert, Nelson Labs

“The Webinar gave me a lot of information around FDA [particularly] on general information/introduction to FDA Overall, [the speaker] was very good in explaining the topics and also in responding to the various questions. It was a useful webinar, and I would recommend it to others who aren't that familiar with the FDA/general legislation.”

Judith Handwerger, Manager Regulatory Affairs, Alfred E. Tiefenbacher (GmbH & Co. KG)