In-house & bespoke training:
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

In-house & bespoke training

A comprehensive introduction to the design and development of medical devices, including device constituent parts of combination products

Rated by attendees to the public programme

Typically presented by David Howlett (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

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An Introduction to the ‘Soft Side’ of Technology Transfers

In-house & bespoke training

The ability to create a working relationship with your partners in a technology transfer is normally overlooked. In the current pharmaceutical landscape, gaining trust should never be an after thought.

Typically presented by Laura Buttafoco (bio)

Delivery: collaborative classroom

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Be In the Know With Pharma 4.0: Building The Business Case For Pharma 4.0

In-house & bespoke training

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.

Typically presented by Lewis Shipp (bio)

Delivery: collaborative classroom

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Be In the Know With Pharma 4.0: Digital CMC

In-house & bespoke training

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.

Typically presented by Lewis Shipp (bio)

Delivery: collaborative classroom

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Be In the Know With Pharma 4.0: Digital Technology Transfer

In-house & bespoke training

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.

Typically presented by Lewis Shipp (bio)

Delivery: collaborative classroom

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

In-house & bespoke training

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.

Typically presented by Koen Cobbaert (bio)

Delivery: collaborative classroom

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Cyber Security for Medical Devices

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Ben Kokx (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

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Data Innovation for AI-enabled Medical Devices

In-house & bespoke training

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.

Typically presented by Koen Cobbaert (bio)

Delivery: collaborative classroom

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

In-house & bespoke training

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.

Typically presented by Koen Cobbaert (bio)

Typical duration: 1 day
Pricing from £450 per attendee
Delivery: collaborative classroom

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

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Richard Featherstone (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

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Innovate: The MedTech Series – Digital Health

In-house & bespoke training

This session will guide participants through the key phases of digital health’s evolution, showcasing real-world cases that illuminate the challenges of  digital adoption.

Typically presented by David Chadima (bio) , Núria Vázquez (bio)

Delivery: collaborative classroom

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Innovate: The MedTech Series – The EU AI Act

In-house & bespoke training

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.

Typically presented by Cheryl Barton (bio)

Delivery: collaborative classroom

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

In-house & bespoke training

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.

Typically presented by Koen Cobbaert (bio)

Typical duration: 2 days
Pricing from £900 per attendee
Delivery: collaborative classroom

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Masterclass: Market Authorisation of AI-enabled Medical Devices

In-house & bespoke training

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.

Typically presented by Koen Cobbaert (bio)

Typical duration: 1 day
Pricing from £450 per attendee
Delivery: collaborative classroom

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Metered Dose Inhaler (MDI) Technology

In-house & bespoke training

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

Rated by attendees to the public programme

Typically presented by David Howlett (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

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

In-house & bespoke training

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

Rated by attendees to the public programme

Typically presented by Anne Jury (bio) , Karen Pearson (bio)

Typical duration: 1 day
Pricing from £450 per attendee
Delivery: collaborative classroom

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Pre-Filled Syringes: End-to-End Processing

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Dale Charlton (bio) , Susanne Hall (bio) , Andreas Rothmund (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

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Smart Packaging and Electronic Patient Information

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Graham Howieson (bio)

Typical duration: 1 day
Pricing from £450 per attendee
Delivery: collaborative classroom

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Sustainable Design and Manufacture for Medical Devices

In-house & bespoke training

Sustainability in medical technology, as in all industries, is increasingly no longer an option. It’s not a question of “if” – it’s a question of “how”. This free webinar will give you a high level of understanding of what sustainability options exist, what the benefits are and what drives them.

Rated by attendees to the public programme

Typically presented by Cormac O'Prey (bio)

Delivery: collaborative classroom

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Sustainable Design and Manufacture for Medical Devices

In-house & bespoke training

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.

Rated by attendees to the public programme

Typically presented by Cormac O'Prey (bio)

Typical duration: 1 day
Pricing from £400 per attendee
Delivery: collaborative classroom

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

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

Good speaker, clearly very knowledgeable in the area. He was happy to have conversations about any specific scenarios/examples/questions we had.
Very friendly and i applaud his speaking almost continuously on this topic for two days

Michaela Hume, Engineer, 42 Technology

As a newcomer to this field, I had hoped for a thorough introduction to Usability Testing. I am pleased to say that my expectations were met. Additionally, I had looked forward to networking, and I found ample opportunity to do so.

Bettina Meervaldt Larsen, Global Trial Manager, Novo Nordisk

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

Good content, covered all aspects that I required.

Anna Short, Design Manager, DM Orthotics

David was a very good presenter in going through the content in detail and made it easy to follow. Great with regards to answering questions people had. Very good webinar for all aspects, would recommend to others

Simran Sandhu, R&D Scientist, Medtrade Products Limited

Very good, lots of relevant material and clearly outlined.

Kurt Blinston, R&D Manager, Medtrade Products Ltd

I was hopping to understand the meaning of Human Factor and Usability in the Generic context and I obtained this knowledge.

Iñigo Gamboa, Medical Advisor, Cinfa S.A.

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