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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

Biopharma

Next events:

  • 20-21 Oct 2025 Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products
  • 10-14 Nov 2025 Biotechnology for the Non-Biotechnologist

See all 9 courses

Clinical Research

Next events:

  • 15-16 Oct 2025 Medical Device Studies: Clinical Evidence
  • 22-24 Oct 2025 Clinical Research Project Management

See all 25 courses

GxP

Next events:

  • 15-16 Oct 2025 Data Integrity Auditor Masterclass
  • 20-21 Oct 2025 Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products

See all 43 courses

Medical Technology

Next events:

  • 3-4 Nov 2025 Smart Packaging and Electronic Patient Information
  • 5-6 Nov 2025 A Practical Overview of Pre-Filled Syringes

See all 20 courses

Medical Writing

Next events:

  • 20-21 Nov 2025 Medical Writing for Medical Devices
  • 23-24 Mar 2026 Successful Medical Writing – from Protocol to CTD

See all 7 courses

Regulatory Affairs

Next events:

  • 8-10 Oct 2025 Pharmaceutical Regulatory Affairs in Asia
  • 15-16 Oct 2025 Variations to Marketing Authorisations

See all 96 courses

Vigilance

Next events:

  • 9-10 Oct 2025 Advanced Pharmacovigilance: From Performing Successful Due Diligence to Benefit-Risk Assessments – What to Consider
  • 15-16 Oct 2025 Advanced Veterinary Pharmacovigilance

See all 29 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...

“An incredible session. The content was relevant, well-structured, and clearly aligned with the audience’s needs. The presentation was engaging and the speaker demonstrated strong expertise and communicated complex ideas in a clear and relatable manner. Overall, the session was highly insightful and impactful. I particularly appreciate the way the speaker explained complex concepts using practical, real-life examples. It made the content much more relatable and easier to understand. The Q&A segment was another highlight—his answers were clear, thoughtful, and directly addressed each question with examples. The overall structure of the session was smooth and engaging, keeping the audience interested from start to finish. It was both informative and interactive.”

Parveen begum Shaik, Head UKPV, Milpharm Limited

“[Speaker was] A very communicative person.”

María López Lago, Regulatory Affairs, CZ Vaccines S.A.U.

“I am very happy with the content of the course. I am sure that my objective to obtain tools for writing and edit texts was achieved successfully.”

María López Lago, Regulatory Affairs, CZ Vaccines S.A.U.

“5-excellent. Practical advices, Real life experience, answers to questions.”

Maria Seifert, Senior Global PV Specialist, Acino AG

“In general I found all quite good. The speaker was quite dynamic, even though he had to present a large amount of content in a short time. He also was receptive to our questions, which is always good. ”

Cecilia Matito, Patent Advisor, Neuraxpharm Pharmaceuticals

“The material was spot-on for bridging the gap between routine PV operations and advanced regulatory preparedness. As someone knee-deep in ICSR processing, I particularly appreciated the deep dives into QMS frameworks

Clear, logical flow with well-paced slides that avoided overload—great for a full-timetable day. Speaker was an absolute expert: confident, relatable, and generous with anecdotes from industry inspections that made the content feel immediate and applicable. Highly recommended for PV professionals looking to strengthen compliance foundations, with minor room for more interactive elements.”

Justin Goh, Senior Safety Data Professional, Lundbeck Singapore Pte. Ltd.

“It was really good for basic knowledge and understanding of PV audit/inspection preparation. The many examples was great.”

Susie Christensen, QPPV and regulatory Affairs specialist, 2care4 Generics ApS

“I was hoping to gain a better understanding of the role of the PRRC, in particular the expectations placed upon them. This was achieved. Overall a very good training session.”

Chris Hooper, Group Quality Manager, Dermal Laboratories Ltd

“Good presenter. ”

Hanne Storgaard, Clinical Quality Operations Lead- Suppliers, MSD Denmark

“good presenter.”

Hanne Storgaard, Clinical Quality Operations Lead- Suppliers, MSD Denmark