Calendar

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

November 2025 training courses

Developing High Performance HR Business Partner and Consulting Skills Training Course

Developing High Performance HR Business Partner and Consulting Skills

4-5 Nov 2025 - London

Learn how to enhance your abilities as an HR business partner and deliver support and a positive impact across any business.

Presented by Katie Botten (bio)

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May 2026 training courses

IP (Intellectual Property) Due Diligence & Freedom to Operate in Practice Training Course

IP Due Diligence & Freedom to Operate in Practice

12 May 2026 - London

This intensive one-day course will give you many insights into the best practice of organising and conducting an efficient and thorough IP due diligence project.

Presented by Tim May (bio)
Andy Spurr (bio)
Tim Whitfield (bio)

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Patent Protection for Software-Related Inventions in Europe and the USA Training Course

Patent Protection for Software-Related Inventions in Europe and the USA

13 May 2026 - London

An intensive update on patent protection for software-related inventions covering all the major developments in European patent law.

Presented by Alan Boyd (bio)
Eileen Brandenburger (bio)
Tim May (bio)

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June 2026 training courses

The Animal Health Summer School: Working Through Veterinary Drug Development in the EU (European Union) and USA Training Course

The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA

15-18 Jun 2026 - London

This practical four-day course provides a comprehensive understanding of veterinary medicine development in the EU and USA.

Presented by Andrew Hewitt (bio)
David Petrick (bio)

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The Art of European Claim Drafting Training Course

The Art of European Claim Drafting

24-25 Jun 2026 - London

This seminar combines one day of claim drafting fundamentals with a further day of focused workshops.

Presented by Joeri Beetz (bio)
Leythem Wall (bio)

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September 2026 training courses

Human Factors and Usability Engineering in the Development of Drug Delivery Products Training Course

Human Factors and Usability Engineering in the Development of Drug Delivery Products

15-16 Sep 2026 - London

This two-day workshop has been designed specifically for product developers who want to incorporate human factors testing into their product development, or need to provide the regulators with specific usability data for their device.

Annual Update for Senior Trade Mark & Design Administrators Training Course

Annual Update for Senior Trade Mark & Design Administrators

30 Sep-1 Oct 2026 - London

This annual update, specifically designed for senior trade mark and design administrators, includes the latest updates from WIPO with discussion on the Madrid and Hague systems and a review of the differences between US, EU and UK practice and what to do about them.

Presented by Xiaodan Dai (bio)
and 7 more leading experts

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November 2026 training courses

Drafting International Intellectual Property Agreements Training Course

Drafting International Intellectual Property Agreements

13 Nov 2026 - London

This course focuses on the drafting skills and legal and commercial issues to be considered when drawing up international IP agreements.

Presented by Anthony D Del Monaco (bio)
Brian Kacedon (bio)
Cara Regan (bio)

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Veterinary Pharmaceutical Submissions in the EU (European Union) Training Course

Veterinary Pharmaceutical Submissions in the EU

19-20 Nov 2026 - London

Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, critical expert reports and regulatory submissions.

Presented by Andrew Hewitt (bio)
Dave Parry (bio)

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Practical Implementation of GCP (Good Clinical Practice) in Veterinary Field Studies Training Course

Practical Implementation of GCP in Veterinary Field Studies

24-25 Nov 2026 - London

This seminar will take many aspects of animal health and veterinary research and development through a typical clinical trial, and pay attention to compliance with Good Clinical Practice (GCP) as outlined in the two guidelines on safety and efficacy produced by FEDESA and the CVMP.

Presented by Rachel Anderson (bio)
Donna Taylor (bio)
Jenny Webster (bio)

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