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:

  • 13-14 May 2025 A Practical Approach to Veterinary Vaccine Development and Registration in the EU
  • 14-15 May 2025 Practical Implementation of GCP in Veterinary Field Studies

See all 12 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:

  • 30 Apr 2025 A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK
  • 20-21 May 2025 Cyber Security for Medical Devices

See all 49 courses

Pharmaceutical

Next events:

  • 8-9 May 2025 Clinical Trial Regulatory Requirements
  • 12 May 2025 An Essential Overview of the Pharmaceutical and Biotech Industries

See all 128 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...

“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

“Overall, this is a good seminar. It is a little long, but that is to be expected looking at the contents and countries to be covered. 5* - I would recommend.”

Kong Kong Weng-Yip, Assistant Manager RA, DUOPHARMA (M) SENDIRIAN BERHAD

“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)

“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)

“The speaker gave a clear presentation that covered all aspects of the training. Overall - good content and presentation, I particularly liked 'technical skills' part. I would recommend, I only suggest shorter exercises at the end of the training.”

Hussein AWADA, Research Scientist, Medincell