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Training courses & Webinars:
Life Sciences

Our life sciences training courses cover Pharmaceuticals, Medical Devices, IVDs, Biotech/Biopharma and Animal Health and have been designed to focus on regulatory affairs, clinical trials, pharmacovigilance, medical writing, latest developments, and best practices (GxP).  Our portfolio of events is extensive and provides training from basic to advanced levels in a variety of formats.  

The pandemic created numerous challenges across all areas of business worldwide and companies had to respond and adapt very quickly. Now, as the healthcare sector emerges stronger and with renewed strategy, life science companies continue to focus on key areas for development, explore the use of emerging technologies, and seek opportunities to harness collaborations and build resilience. 

 

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:

  • 25-26 Nov 2025 Practical Implementation of GCP in Veterinary Field Studies
  • 25-26 Nov 2025 Veterinary Pharmaceutical Submissions in the EU

See all 17 courses

Biopharma

Next events:

  • 26 Nov 2025 US FDA - Understanding Key Factors When Working with the FDA
  • 16-17 Mar 2026 Biosimilars

See all 11 courses

Clinical Research

Next events:

  • 25-26 Nov 2025 Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
  • 25-26 Nov 2025 Practical Implementation of GCP in Veterinary Field Studies

See all 21 courses

Cosmetics

Next events:

  • 18-19 Jun 2026 Cosmetovigilance
  • 8-9 Dec 2026 Cosmetovigilance

See all 2 courses

GxP

Next events:

  • 24-25 Nov 2025 The Common Technical Document
  • 24-25 Nov 2025 Understanding Computer System Validation (CSV)

See all 35 courses

Medical Devices

Next events:

  • 25-26 Nov 2025 Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
  • 2-3 Dec 2025 FDA Approval Process for Medical Devices

See all 52 courses

Medical Technology

Next events:

  • 3-4 Dec 2025 An Introduction to the Design and Development of Medical Devices
  • 26-30 Jan 2026 Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations

See all 15 courses

Medical Writing

Next events:

  • 23-24 Mar 2026 Successful Medical Writing – from Protocol to CTD
  • 15 May 2026 Effective Technical Writing & Editing

See all 6 courses

Pharmaceutical

Next events:

  • 24-25 Nov 2025 The Common Technical Document
  • 24-25 Nov 2025 Understanding Computer System Validation (CSV)

See all 109 courses

Regulatory Affairs

Next events:

  • 24-25 Nov 2025 The Common Technical Document
  • 24-25 Nov 2025 Understanding Computer System Validation (CSV)

See all 90 courses

Vigilance

Next events:

  • 1-2 Dec 2025 Pharmacovigilance Aspects of Licensing Agreements
  • 2-3 Feb 2026 Signal Detection and Regulatory Expectations

See all 23 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 was hoping to have a detailed analysis of all the aspects a legal who works in a pharmaceutical company may encounter and how to deal with it. I must say the webinar was very beyond my expectations and I definitely accomplished my goal (and more!). I am in the pharmaceutical industry just from 2022, and this two days helped me a lot. ”

Margherita Aina, Legal Specialist, NTC S.r.l.

“My vote is definitely a 10/10: the webinar dealt with all the topics (and more..) I wanted to explore, as I work with it every day. I liked a lot also all the PPT presentations. All speakers were excellent, and the way of explaining very clear and prepared. I found the topics very engaging.”

Margherita Aina, Legal Specialist, NTC S.r.l.

“I manage externals who work for/with my colleagues in the field of veterinary vaccines. In order to better understand their daily work, I attended this training. I think I can now better understand what my colleagues and our external partners have to do with RA activities for vaccines. I liked that I was able to work well in the SPC workshop regarding "Wondabov" despite my limited experience. That was very gratifying and motivating. [Speakers] were both very nice. ”

Vanessa Efinger, Manager RA Outsourcing, Boehringer Ingelheim Vetmedica GmbH

“This seminar provided excellent teaching thanks to an impeccable structure and engaging speakers. I learned a lot. The volume of information was dense, but the clarity of the organization makes it perfectly exploitable in deferred viewing. It is an ideal resource for modular and punctual consultation depending on requirements. I most appreciated the listing of applicable regulatory guidances, as I know I will frequently refer to them in my work. The practical exercise was also excellent for solidifying the theory previously learned.”

Mélodie Métayer, Regulatory Affairs Executive EU, Virbac Corp

“I manage externals who work for/with my colleagues in the field of veterinary vaccines. In order to better understand their daily work, I attended this training. I think I can now better understand what my colleagues and our external partners have to do with RA activities for vaccines. I liked that I was able to work well in the SPC workshop regarding "Wondabov" despite my limited experience. That was very gratifying and motivating. [Speakers] were both very nice. ”

Vanessa Efinger, Manager RA Outsourcing, Boehringer Ingelheim Vetmedica GmbH

“This seminar provided excellent teaching thanks to an impeccable structure and engaging speakers. I learned a lot. The volume of information was dense, but the clarity of the organization makes it perfectly exploitable in deferred viewing. It is an ideal resource for modular and punctual consultation depending on requirements. I most appreciated the listing of applicable regulatory guidances, as I know I will frequently refer to them in my work. The practical exercise was also excellent for solidifying the theory previously learned.”

Mélodie Métayer, Regulatory Affairs Executive EU, Virbac Corp

“A good concentrated overview of the topic of drafting pharma contracts which is normal for a 2 day course in the subject. I enjoyed the overall experience.”

Larissa Toribio-Monnay, Manager Paralegal & Contract Management , Fresenius Kabi SwissBioSim GmbH

“Very well organised, to time, good content, and well delivered. [Speaker] was engaging and delivered a really good balance between lecture content and breakout sessions. I had already done project management training and was hoping to get more of an insight into practical implementation of techniques. The course was very good at this, with multiple breakout sessions to practice this implementation.”

Joe Cartwright, Head of Projects, University of Sheffield

“I appreciated the fact that we could easily ask questions without feeling embarrassed. The speakers were very friendly. It was very interesting and understandable. I think we were provided with a lot of content, that I will certainly use in the future.”

Marine Cassisi, Regulatory Affairs Officer, Virbac Corp

“I appreciated the fact that we could easily ask questions without feeling embarrassed. The speakers were very friendly. It was very interesting and understandable. I think we were provided with a lot of content, that I will certainly use in the future.”

Marine Cassisi, Regulatory Affairs Officer, Virbac Corp