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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:

  • 10-14 Nov 2025 Biotechnology for the Non-Biotechnologist
  • 10-11 Nov 2025 Stability Testing of Pharmaceuticals and Biopharmaceuticals

See all 13 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:

  • 10-11 Nov 2025 Stability Testing of Pharmaceuticals and Biopharmaceuticals
  • 24-25 Nov 2025 The Common Technical Document

See all 36 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 53 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:

  • 10-14 Nov 2025 Biotechnology for the Non-Biotechnologist
  • 10-11 Nov 2025 Stability Testing of Pharmaceuticals and Biopharmaceuticals

See all 113 courses

Regulatory Affairs

Next events:

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

See all 91 courses

Vigilance

Next events:

  • 12 Nov 2025 A Practical Guide to Writing Risk Management Plans (RMPs)
  • 1-2 Dec 2025 Pharmacovigilance Aspects of Licensing Agreements

See all 24 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...

“The content, the presentation, and the presenter were all excellent. Standard requirements for the gamma sterilization process part of the training was very detailed and helped me a lot in understanding the expectations.”

Daniella Alberti-Juhász , Microbiologist, Medicontur Medical Engineering Ltd

“The content, the presentation, and the presenter were all excellent. Standard requirements for the gamma sterilization process part of the training was very detailed and helped me a lot in understanding the expectations.”

Daniella Alberti-Juhász , Microbiologist, Medicontur Medical Engineering Ltd

“The content, the presentation, and the presenter were all excellent. Standard requirements for the gamma sterilization process part of the training was very detailed and helped me a lot in understanding the expectations.”

Daniella Alberti-Juhász , Microbiologist, Medicontur Medical Engineering Ltd

“ Content was good, speaker was knowledgeable and the pace was good.”

Richard Pringle, Associate Director of Regulatory Affairs, Univet Ltd

“I was hoping to gain a better understanding of regulatory variations, and the webinar was very useful, clear and comprehensive. It will definitely help me in my work. I appreciated that speaker was interactive with the class and very kind.”

Maria Pina Desiante, PV Scientist, APL Swift Services Ltd

“I was hoping to gain a better understanding of regulatory variations, and the webinar was very useful, clear and comprehensive. It will definitely help me in my work. I appreciated that speaker was interactive with the class and very kind.”

Maria Pina Desiante, PV Scientist, APL Swift Services Ltd

“Generally it was good.”

Sandra Nicoll, Director Regulatory Affairs & Quality UK & Ireland, Alexion Pharma UK Ltd

“Very good and very clear ”

Brian Mzila, Quality Manager, Alexion Pharma UK Ltd

“Generally it was good.”

Sandra Nicoll, Director Regulatory Affairs & Quality UK & Ireland, Alexion Pharma UK Ltd

“Very good and very clear ”

Brian Mzila, Quality Manager, Alexion Pharma UK Ltd