Technology and innovation in the medical device and pharmaceutical industries is constantly changing, from innovation in products to improving existing products, new manufacturing processes, and modes of practice.
Our medical technology training courses will provide delegates with essential information, illustrate the opportunities available from the use of medical device software to artificial intelligence, and keep you abreast of the evolving regulations.
Our expert faculty of speakers will also present developments in specific therapeutic areas.
Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book
1-2 Apr 2025 - Online webinar
Also on: 23 Jul 2025
A comprehensive introduction to the design and development of medical devices, including device constituent parts of combination products
Presented by David Howlett (bio)
16 Sep 2025 - Online webinar
This course will equip you with the tools and insights needed to articulate your vision, secure funding, and pave the way for Pharma 4.0 success.
Presented by Lewis Shipp (bio)
19 Mar 2025 - Online webinar
Also on: 23 Sep 2025
Through this interactive session, participants will explore the forces driving the shift toward digital transformation, understand the challenges Digital CMC addresses, and learn about its operational and regulatory advantages.
Presented by Lewis Shipp (bio)
9 Sep 2025 - Online webinar
This course explores how leveraging digital solutions, companies can not only accelerate the transfer of critical knowledge but also foster innovation and gain an edge in increasingly competitive markets.
Presented by Lewis Shipp (bio)
9 Jul 2025 - Online webinar
Also on: 12 Nov 2025
Master the complexities of software classification under the Medical Device Regulations (MDR), ensuring compliance and clarity with expert insights into Medical Device Coordinators Group (MDCG) guidelines. Regulatory frameworks will be discussed and practical case studies will be included (to aid the learning process).
Presented by Koen Cobbaert (bio)
8-9 May 2025 - Online webinar
Also on: 11 Sep 2025
This seminar will provide you with an understanding of cybersecurity and its increasing regulatory focus, and how to embed and apply state-of-the-art security in your existing processes to deliver safe and secure products and solutions.
Presented by Ben Kokx (bio)
9 Jul 2025 - Online webinar
Also on: 12 Nov 2025
This course provides an in-depth understanding of data governance for AI-enabled medical devices, focusing on European regulations like the AI Act and GDPR, ensuring compliance while fostering innovation in high-risk AI systems.
Presented by Koen Cobbaert (bio)
10 Jul 2025 - Online webinar
Also on: 13 Nov 2025
Gain essential knowledge in developing and managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW), focusing on regulatory compliance, risk management, and lifecycle management to ensure safety and effectiveness.
Presented by Koen Cobbaert (bio)
13-14 May 2025 - Online webinar
Also on: 16 Sep 2025
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)
15 May 2025 - Online webinar
Also on: 7 Nov 2025
This session, in partnership with Bax Innovation, will guide participants through the key phases of digital health’s evolution, showcasing real-world cases that illuminate the challenges of digital adoption.
3 Apr 2025 - Online webinar
Also on: 2 Oct 2025
This session will summarise the EU AI Act and its implications on the healthcare sector, including how to be compliant with the new regulatory framework.
Presented by Cheryl Barton (bio)
7-8 Jul 2025 - Online webinar
Also on: 10 Nov 2025
Learn the critical regulatory requirements and best practices for obtaining market authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) in global markets.
Presented by Koen Cobbaert (bio)
4 Apr 2025 - Online webinar
Also on: 11 Jul 2025
This course provides essential guidance on navigating regulatory requirements and securing market authorisation for AI-based medical devices, covering key regulations, compliance strategies, and best practices for global market access.
Presented by Koen Cobbaert (bio)
19-20 Jun 2025 - Online webinar
Also on: 8 Oct 2025
A comprehensive overview of MDIs including development, manufacture, regulation and market potential
Presented by David Howlett (bio)
5 Jun 2025 - Online webinar
Also on: 9 Oct 2025
In this practical, one-day course, learn the regulatory requirements needed for successful post-market surveillance of medical devices and IVDs.
21-22 Jul 2025 - Online webinar
Also on: 5 Nov 2025
Topics such as quality of syringe manufacture, quality of syringe components and why, quality of filling (volume check, reject reduction), quality of inspection and product release will be discussed in detail.
3 Jul 2025 - Online webinar
Also on: 3 Nov 2025
This course will provide an overview of the current technologies, the patient and societal benefits and some building blocks for the establishment and delivery of e-PIL and SMART strategic initiatives.
Presented by Graham Howieson (bio)
3 Jul 2025 - Online webinar
Also on: 27 Nov 2025
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)
14 May 2025 - Online webinar
Also on: 10 Sep 2025
This course will help you understand future manufacturing of medical devices using 3D printing technology. Anyone from the medical device, additive manufacturing and pharmaceutical industries will benefit.
Presented by Ruchi Pathak (bio)