Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book
8-9 Sep 2025 - 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
16-17 Sep 2025 - 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.
Presented by Richard Featherstone (bio)
22-23 Sep 2025 - London
Gain a comprehensive understanding of the EU and FDA process validation guidance, learn how to establish a process validation programme, understand the link between QbD and process validation, apply relevant tools for process validation including risk assessment.
Presented by Bruce Davis (bio)
25-26 Sep 2025 - London
This prestigious ‘must-attend’ event has been designed specifically for senior patent administrators. It provides an ideal opportunity to learn about developments that affect you and your role, to make sure you are up to date on best-practice and are working as efficiently as possible.
14 Oct 2025 - London
To defend your client's interests correctly and competently it is vital to know what to expect at oral proceedings and to be property prepared.
Presented by Joeri Beetz (bio)
4 Nov 2025 - London
This seminar provides a comprehensive overview of the principles of patent claim interpretation in the USA, UK and Germany.
5-6 Nov 2025 - London
This seminar addresses the parallel, but substantially different, rules for drafting and prosecuting patents required by the Examiners and Appeal Boards of the EPO and USPTO.
11-12 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)
25-26 Nov 2025 - 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.
25-26 Nov 2025 - 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.
27 Nov 2025 - London
This seminar will give you an in-depth understanding of what sustainability options exist, what the benefits are, what drives them, and how to choose which will work for your company.
Presented by Cormac O'Prey (bio)