Home
Life Sciences

In-house & bespoke training:
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

Sample course outlines include:

Biosimilars
Biotechnology for the Non-Biotechnologist

See all 8 course outlines

Clinical Research

Sample course outlines include:

Advanced Project Management in Clinical Research
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects

See all 24 course outlines

GxP

Sample course outlines include:

A Practical Introduction to Good Clinical Practice (GCP)
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices

See all 56 course outlines

Medical Technology

Sample course outlines include:

A Practical Overview of Pre-Filled Syringes
An Introduction to the Design and Development of Medical Devices

See all 20 course outlines

Medical Writing

Sample course outlines include:

Achieving Publication Success in Scientific Journals
Dealing With Scientific Journal Reviewers: From Comments to Resubmission

See all 13 course outlines

Regulatory Affairs

Sample course outlines include:

A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products
A Practical Approach to Veterinary Vaccine Development and Registration in the EU

See all 72 course outlines

Vigilance

Sample course outlines include:

A Practical Guide to Producing and Maintaining the PSMF
A Practical Guide to Writing Risk Management Plans (RMPs)

See all 23 course outlines

Training options

All of our course outlines are available:
	Ready made for any number of participants	or		With a programme and presenters customised to your requirements
And in your preferred format, or combination:
	Face-to-face training at your location	or		Webinar/interactive online

“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