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:

  • 3-4 Jul 2025 Introduction to Veterinary Pharmacovigilance
  • 15-16 Oct 2025 Advanced Veterinary Pharmacovigilance

See all 7 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:

  • 13-14 Oct 2025 Cosmetovigilance

See 1 course

Medical Devices

Next events:

  • 19-20 Jun 2025 Metered Dose Inhaler (MDI) Technology
  • 26 Jun 2025 UK Conformity Assessed (UKCA) Marking for Medical Devices

See all 38 courses

Pharmaceutical

Next events:

  • 16-17 Jun 2025 MBA Strategic Thinking for Pharma and Biopharma Professionals
  • 16-17 Jun 2025 Understanding Pharmacovigilance Regulations in APAC

See all 96 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...

“I accomplished a better understanding on the role of the PRRC. Very knowledgeable [speaker] with a good presentation style.”

Adrian Dunleavy, UK Quality & Regulatory Manager, Freudenberg Performance Materials LP

“I hoped to improve my knowledge in the field of in-licensing and out-licensing agreements. I am completely satisfied. I got answers to my questions, structured my knowledge, received new, previously unknown to me information Everything was great.”

Karīna Kudore, Lawyer, Olpha

“Very concentrated and structured content. All speakers had high level expertise on the topics presented. Useful for in-house practitioners (lawyers, BD) in the pharmaceutical industry as a guide to the main topics in contract drafting. I have expanded my knowledge [on] license agreement issues, IP issues, Co-development agreements.”

Lana Zida, Lawyer, Olpha

“It was well laid out and formatted especially for myself who does not have a regulatory role currently. I was hoping to achieve a firmer understanding and overview of submission within the EU, and believe I achieved this. [Speakers] were very knowledgable and provided great answers to all questions— supportive but challenged us when doing the workshop. I liked all areas of the course.”

Louise Dunn, Pharmacovigilance and Technical advisor, Zoetis

“Excellent. I was hoping to refresh, add to and update my knowledge. The webinar was excellent to remind me of areas that I had been involved with many years ago and add knowledge that is more relevant to my role now. I found the topics of the workshop particularly relevant.”

Mary-Ann Tite, Regulatory Manager, Pets |Choice

“Fantastic webinar! Speakers were very knowledgeable, clear, concise, and open to questions at any time—providing in depth background information were appropriate as well. The content was very interesting and I think a very good amount was covered considering the timescales. I enjoyed the workshop a lot. I thought it was a good way to try and put into practice what we had learnt during the webinars. I also thought a very good amount of information was covered for an introduction into the sections of the dossier.”

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

“My goal was to gain a deeper awareness and understanding of what is required in the different sections of a dossier for submission in the EU. I think the course definitely accomplished this and there was lots of useful information, which was very well explained. I can confidently say that I left knowing a lot more than I initially thought I would.”

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

“Loved it. Great content, great presenter/instructor. He was engaging and explained things clearly, answering questions along the way. I particularly liked the way he brought the content to life and gave greater insight through sharing examples of his personal experiences. Great course, would recommend.”

Kishori Amatya, PV and MI officer, Jenson R+

“The webinar is well constructed and the speaker is a very polite and prepared person. I managed to get the initial information needed to start studying and understanding the process validation program, the exercises [were] very helpful.”

Alessandra Fanzini, CDMO, REITHERA SRL

“I really enjoyed this webinar. I will be recommending it to colleagues as a great source of information and introduction to process validation. The material was engaging, and [speakers'] knowledge/experience was communicated very well. I greatly enjoyed the content and presentation style. Topics were split up and presented in a logical order and the exercises were very helpful to reiterate the information that was presented.”

Brianna Boehm, Process Validation Technical Writer, Aldevron