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
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |