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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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: 1 day
Pricing from £800 per attendee
Delivery: collaborative classroom

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Drug Discovery: A Step-by-Step Introduction

In-house & bespoke training

This drug discovery training course takes you on a science-based drug discovery journey. You will travel from inception of a new project to the point of hand-over of the newly discovered molecule to the Drug Development Team for pre-clinical and clinical studies. The course breaks down the long, multi-faceted drug discovery process into individual steps which build towards this key goal. The focus is on how essential science, technology and infrastructure elements are constituted, deployed and integrated to maximise the likelihood of a successful drug discovery project.

Typically presented by Peter A. Lowe (bio)

Typical duration: 2 days
Delivery: collaborative classroom

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

In-house & bespoke training

Applying HF and usability to comply with the MDR.

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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Masterclass: Artificial Intelligence-based Medical Devices

In-house & bespoke training

Many companies take part in the global ‘race to AI’ by continuously broadening the role of AI in their product portfolio. However, the rules of the game appear to be changing. The increased visibility of the technology’s risks has led to calls for regulators to look beyond the benefits, and also secure appropriate legislation to ensure AI that is ‘trustworthy’– legal, ethical, and robust and to ensure data is portable and qualitative. During this session, we will discuss the main players, trends, and challenges in the ‘race’ to AI regulation and how companies can move forward with an advantage.

Rated by attendees to the public programme

Typically presented by Koen Cobbaert (bio)

Typical duration: 3 days
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: 3 days
Pricing from £1,200 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

Understanding the regulatory requirements for successful post-market surveillance of medical devices and IVDs is increasingly important and practical application of the regulations is key to a successful PMS system.
This course will provide a clear understanding of the intention of the requirements, and discuss the responsibilities of the manufacturer, notified bodies and competent authorities.

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

Typical duration: 1 day
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)
and 3 more leading experts

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

Increased use of SMART technologies has become ever more prevalent in the delivery of healthcare solutions as well as in the electronic delivery of Patient Information (e-PIL) and leaflets (e-leaflets). 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, providing insight as to where organisations may be most significantly impacted.

Typically presented by Graham Howieson (bio)

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

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 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. It will also provide practical advice on how to implement change.

Rated by attendees to the public programme

Typically presented by Cormac O'Prey (bio)

Delivery: collaborative classroom

More @ IPI Academy

Excellent, it was very interesting and I find the speaker very knowledgeable.

Kolbrun E Ottosdottir, , Nox Medical

Richard is very knowledgeable in the topic and was able to answer all questions by providing both regulatory references and examples which made understanding requirements easier.

Geno Govender, Senior Manager - Quality Devices, Vectura Limited

I was looking for the exact standards what we could apply for our Device Cyber Security Perspective and how we could document Cybersecurity in Regulatory Documents (Risk Assessment, GSPR etc.) Training was helpful, now we could conclude which standard and how we could comply in our documents.

Meenakshi Kamboj, Senior Regulatory Specialist - Development • Regulatory, Flexicare Ltd

Very knowledgeable, up to date on things in this field even parts you usually do not get a glimpse in. An excellent program.

Harpa Arnardóttir, Chief Quality Officer, Nox Medical

Very passionate and answered questions clearly

Genn Kamei, , Nox Medical

Extremely knowledgeable and capable presenters with very informative and well delivered content.

Derek Hoogerbrugge, , Accenture UK Ltd

Richard was very keen of answering any questions coming from the participants and trying to adapt the training course to the participants needs/requests.

J.Ignasi Escamilla, Device Development Advisor, Ferrer Internacional S.A.

I really appreciated the rich content of the slides, the level of information provided and the very clear overview of the regulator context, and the roadmaps.

Alexia Pleinecassagne, RAQA Specialist, Medimaps Group SA

The course was well structured, in depth, and clearly from an expert in the field. Threat modelling was very helpful.

Richard Hoodless, Principal Engineer, ATL technology

Very knowledgeable provided a very good insight.

Mike Ibbotson, Embedded Engineer, ATL Technology Ltd