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

A Practical Overview of Pre-Filled Syringes

In-house & bespoke training

Master pre-filled syringe manufacturing, quality control, and regulatory compliance in this comprehensive 2-day course. Includes hands-on workshops, expert insights, and CPD certification.

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 £1,000 per attendee
Delivery: collaborative classroom

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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 £1,000 per attendee
Delivery: collaborative classroom

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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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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 Medical Device Coordinators Group (MDCG) guidelines. Regulatory frameworks will be discussed and practical case studies will be included (to aid the learning process).

Typically presented by Koen Cobbaert (bio)

Typical duration: Half-day days
Pricing from £350 per attendee
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 £1,000 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)

Typical duration: Half-day days
Pricing from £350 per attendee
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 £500 per attendee
Delivery: collaborative classroom

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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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Digital Technology Transfers

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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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

Typical duration: 2 days
Pricing from £1,000 per attendee
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 requirements and best practices for obtaining market authorisation of 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 £1,000 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 authorisation for AI-based medical devices, covering key regulations, compliance strategies, and best practices for global market access.

Rated by attendees to the public programme

Typically presented by Koen Cobbaert (bio)

Typical duration: 1 day
Pricing from £500 per attendee
Delivery: collaborative classroom

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Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations

In-house & bespoke training

An introduction to medical device software regulations and requirements to include the latest EU and FDA guidance and risk management.

Rated by attendees to the public programme

Typically presented by Koen Cobbaert (bio) , Zuzanna Kwade (bio)

Typical duration: 5 days
Pricing from £1,875 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 £1,000 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 £500 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 £500 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 Product Design for MedTech Engineers and Developers

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: 2 days
Pricing from £1,000 per attendee
Delivery: collaborative classroom

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The 2024 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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The Future of Manufacturing: 3D Printing for Medical Devices

In-house & bespoke training

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.

Typically presented by Ruchi Pathak (bio)

Typical duration: 1 day
Pricing from £500 per attendee
Delivery: collaborative classroom

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Overall this course was excellent, and I found it extremely useful. I would highly recommend it. I wanted to understand the processes for developing compliant medical device software. I definitely got the necessary information to understand this better. Both excellent speakers and clearly extremely knowledgeable on the subject matter. Very impressive. I thought it would focus more on the development process (e.g. detail around how to implement EN 62304), but what this course demonstrated was that there is a lot more to consider. So that was a useful learning experience as well.

Tom Clarke, Director, ISO Sense Consulting Ltd.

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

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

It was a nice course to follow as a junior HF engineer I would absolutely recommend it.

Sofia Poletto, Human Factors Engineer, Chiesi Farmaceutici SPA

Overall very good.

William Hensler, Principal, Alantra BioPharma

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

Wicem Boumalouka, Chef de Projet, Guerbet LLC

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 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

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