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Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book

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 10 course outlines

Sample course outlines include:

  • US FDA - Understanding Key Factors When Working with the FDA

See 1 course outline

Sample course outlines include:

  • Cosmetovigilance
  • Regulatory Compliance and Safety Standards for Aesthetic Devices

See all 2 course outlines

Sample course outlines include:

  • A Practical Overview of Pre-Filled Syringes
  • A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

See all 59 course outlines

Sample course outlines include:

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

See all 142 course outlines

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