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
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 |
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 |
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 |
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 |
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 |
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
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 |
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 |
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.
Rated by attendees to the public programme
Typically presented by Graham Howieson (bio)
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
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 |