Training courses & Webinars:
Medical Technology

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

An Introduction to the Design and Development of Medical Devices Training Course

An Introduction to the Design and Development of Medical Devices

8-9 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)

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Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Training Course

Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW)

28 Feb 2025 - Online webinar
Also on: 9 Jul 2025

Master the complexities of software classification under the Medical Device Regulations (MDR), ensuring compliance and clarity with expert insights into MDCG guidelines, practical case studies, and regulatory frameworks.

Presented by Koen Cobbaert (bio)

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Cyber Security for Medical Devices Training Course

Cyber Security for Medical Devices

28-29 Jan 2025 - Online webinar
Also on: 8 May 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)

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Data Innovation for AI-enabled Medical Devices Training Course

Data Innovation for AI-enabled Medical Devices

28 Feb 2025 - Online webinar
Also on: 9 Jul 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)

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Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Training Course

Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW)

3 Mar 2025 - Online webinar
Also on: 10 Jul 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)

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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

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)

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Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Training Course

Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW)

26-27 Feb 2025 - Online webinar
Also on: 7 Jul 2025

Learn the critical regulatory requirments and best practices for obtaining market authorisation or Software as a Medical Device (SaMD) and Medical Device Software (MDSW) in global markets.

Presented by Koen Cobbaert (bio)

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Masterclass: Market Authorisation of AI-enabled Medical Devices Training Course

Masterclass: Market Authorisation of AI-enabled Medical Devices

4 Apr 2025 - Online webinar
Also on: 11 Jul 2025

This course provides essential guidance on navigating regulatory requirements and securing market authorization for AI-based medical devices, covering key regulations, compliance strategies, and best practices for global market access.

Presented by Koen Cobbaert (bio)

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Metered Dose Inhaler (MDI) Technology Training Course

Metered Dose Inhaler (MDI) Technology

24-27 Feb 2025 - Online webinar
Also on: 19 Jun 2025

A comprehensive overview of MDIs including development, manufacture, regulation and market potential

Presented by David Howlett (bio)

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Post-Market Surveillance - Practical Application for Medical Devices and IVDs Training Course

Post-Market Surveillance - Practical Application for Medical Devices and IVDs

12 Feb 2025 - Online webinar
Also on: 5 Jun 2025

In this practical, one-day course, learn the regulatory requirements needed for successful post-market surveillance of medical devices and IVDs.

Presented by Anne Jury (bio)
Karen Pearson (bio)

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Pre-Filled Syringes: End-to-End Processing Training Course

Pre-Filled Syringes: End-to-End Processing

20-21 Mar 2025 - Online webinar
Also on: 21 Jul 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.

Presented by Dale Charlton (bio)
Susanne Hall (bio)
Andreas Rothmund (bio)

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Smart Packaging and Electronic Patient Information Training Course

Smart Packaging and Electronic Patient Information

13 Mar 2025 - Online webinar
Also on: 3 Jul 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)

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Sustainable Design and Manufacture for Medical Devices Training Course

Sustainable Design and Manufacture for Medical Devices

24 Mar 2025 - Online webinar
Also on: 3 Jul 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)

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It was good.

Shubhangi Chouhan, Regulatory Affairs Specialist, Mölnlycke Health Care AB

It was an enlightening course, and the speakers were so explanatory.

Stergios Kemidis, Head of R&D, ANFARM HELLAS S.A.

Koen is a great speak who explains things very clearly with examples

Yisong Yin, Software Regulatory Affairs Specialist, Convatec

Great knowledge of the material. Great speaker. I liked when the speaker gave insights into what will be expected of manufacturers and what legislation or publications are coming down the line and also his insights into the future

Denise McDermott, Regulatory Compliance Team lead, Compliance and Risks

Koen is a great speak who explains things very clearly with examples

Yisong Yin, Software Regulatory Affairs Specialist, Convatec

It was really good, both speakers tried to keep the audience attention with interactive tasks. As an overall view I am satisfied with the webinar and with the provided training materials, both with the shared information and the information quality.

Szilvia Schmidt, AMD Technical Specilaist, B.Braun Medical Hungary Ltd

[Speakers had] huge expertises. I accomplished what I wanted to achieve from this course.

Wicem Boumalouka, Chef de Projet, Guerbet LLC

Speakers were very knowledgeable and openly shared their experience with the audience especially when asked about specific examples.

Natalia Harasimiuk, Associate Director, Fuji Film

[Speaker was] very friendly, very knowledgeable.

Karen Ellis, Artwork Implementation Specialist, Theramex Pharmaceuticals

The webinar was very interesting, good discussions. The examples of smart packaging I liked.

Chantal Mutsaers, Senior Manager Scientific and Procedural Regulatory Affairs, PHARA PLUS LIFE SCIENCE SERVICES BV