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Training courses & Webinars:
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
24-25 Jul 2024 - Online webinar
Also on: 10 Dec 2024
A comprehensive introduction to the design and development of medical devices, including device constituent parts of combination products
Presented by David Howlett (bio)
Cyber Security for Medical Devices
4-5 Jul 2024 - London
Also on: 15 Oct 2024
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.
Presented by Ben Kokx (bio)
Drug Discovery: A Step-by-Step Introduction
23-24 Sep 2024 - Online webinar
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.
Presented by Peter A. Lowe (bio)
Human Factors and Usability Engineering in the Development of Drug Delivery Products
5-6 Jun 2024 - London
Also on: 17 Sep 2024
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.
Presented by Richard Featherstone (bio)
Masterclass: Artificial Intelligence-based Medical Devices
26 Jul 2024 - Online webinar
Also on: 7 Nov 2024
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.
Presented by Koen Cobbaert (bio)
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
22-25 Jul 2024 - Online webinar
Also on: 9 Dec 2024
An introduction to medical device software regulations and requirements to include the latest EU and FDA guidance and risk management.
Metered Dose Inhaler (MDI) Technology
20-21 Jun 2024 - Online webinar
Also on: 9 Oct 2024
A comprehensive overview of MDIs including development, manufacture, regulation and market potential
Presented by David Howlett (bio)
Post-Market Surveillance - Practical Application for Medical Devices and IVDs
6 Jun 2024 - Online webinar
Also on: 10 Oct 2024
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.
Pre-Filled Syringes: End-to-End Processing
25-26 Jul 2024 - Online webinar
Also on: 6 Nov 2024
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.
Presented by
Dale Charlton (bio)
and 3 more leading experts
Smart Packaging and Electronic Patient Information
10 Jul 2024 - Online webinar
Also on: 4 Nov 2024
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.
Presented by Graham Howieson (bio)
Sustainable Design and Manufacture for Medical Devices
4 Jul 2024 - Online webinar
Also on: 4 Oct 2024
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.
Presented by Cormac O'Prey (bio)