Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book
12-13 May 2025 - London
This two-day course provides an introduction to pharmaceutical regulatory affairs and the basics of drug development and has been designed specifically for those working in a support staff role.
Presented by Norah Lightowler (bio)
13 May 2025 - London
This seminar provides a comprehensive overview of the principles of patent claim interpretation in the USA, UK and Germany.
14-15 May 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.
22 May 2025 - London
This one day course will cover the role of the Person Responsible for Regulatory Compliance (PRRC) introduced by the implementation of the Medical Device Regulation 2017/745 and the In-Vitro Diagnostic Device Regulation 2017/746. The course will review Article 15 from the regulation in detail to enable understanding of the intent of each requirement. It will also present the UK Medical Device Regulation requirements and discuss the proposed Qualified Person role with current information.
Presented by Stuart Angell (bio)
2-3 Jun 2025 - London
The ‘how to’ of technology transfer across the product lifecycle.
Presented by Bruce Davis (bio)
9-13 Jun 2025 - London
This comprehensive course has been designed to map the processes from device concept to marketing and show how regulatory, quality, clinical and other aspects of device development are joined into a continuous process.
Presented by
Stuart Angell (bio)
and 7 more leading experts
16-19 Jun 2025 - London
This practical four-day course provides a comprehensive understanding of veterinary medicine development in the EU and USA.
1 Jul 2025 - 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.
2-4 Jul 2025 - London
This course will be of maximum benefit to those drug safety professionals who are working both in the clinical and post-marketing safety arena including QA for auditing.
Presented by Graeme Ladds (bio)
2 Jul 2025 - London
An intensive update on patent protection for software-related inventions covering all the major developments in European patent law.
9 Jul 2025 - London
This course will cover the key regulations used globally in human factors and usability engineering: the specific standards and guidances, methods, and the tools commonly used in medical device development.
Presented by Greg Thay (bio)
9-11 Jul 2025 - London
An ideal course for non-scientists and scientists who need to understand the basic theory, principles, techniques and potential of biotechnology.
Presented by
Robert Alvarez (bio)
and 6 more leading experts
14-18 Jul 2025 - London
An intensive 5-day course that will give you a valuable insight and a comprehensive understanding of the European Patent Office processes.
Presented by
Joeri Beetz (bio)
and 3 more leading experts
14-15 Jul 2025 - London
This two-day seminar for administrative staff in the patent profession details how to competently prepare an application for filing before the EPO.
*INCLUDES: Practical and interactive exercises*
Presented by Richard Gillespie (bio)
16-17 Jul 2025 - London
This seminar combines one day of claim drafting fundamentals with a further day of focused workshops.
18 Jul 2025 - London
Clarity in drafting patent applications has always been a serious issue. The purpose of the seminar is to teach delegates the essentials of clarity and the most effective use of the problem-solution approach, giving delegates an edge over other parties.
*INCLUDES: Interactive workshop sessions and details of the latest case law and its implications*
Presented by Daniel X Thomas (bio)
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)
24-26 Sep 2025 - London
This course provides an essential overview of pharmaceutical packaging and will be valuable for newcomers to this field. It will also act as a good refresher for those with more experience.
Presented by Chris Penfold (bio)
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
Achieve excellence as an HR business partner and enhance your ability to deliver a positive impact and support across the whole business.
Presented by Katie Botten (bio)
13 Nov 2025 - London
This course focuses on the drafting skills and legal and commercial issues to be considered when drawing up international IP agreements.
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)