ITL Group

ITL Group (a G&H company) is the award-winning medical device design, development and manufacturing partner of life-saving medical technology, diagnostic devices and analytical instruments.

Established in 1977, ITL Group, based in Kent, have worked on more than 400 projects at various stages of their product development life-cycle.

With clients ranging from one-man start-ups to world-leading organisations, ITL have the capability to take your project from conceptualisation all the way through to full scale manufacture and aftersales support as part of our complete product development service.

Our facilities in the UK, USA and China enable us to offer our clients world-wide support and access to global supply chains and markets.

At ITL we approach things a little differently than the average contract design and manufacturing partner, and believe in working with, and not simply for, our clients.

ITL Group is audited and accredited to ISO 9001, ISO 13485 and FDA CFR 21 part 820.

ITL are proud to maintain a highly controlled Quality Management System to assist you in the design, development and manufacture of medical products for worldwide markets

BSI Assurance Mark ISO 9001 & ISO 13485

“Bedfont have built a good working relationship with ITL whilst creating two of our most successful product launches to date. Given the nature of our specialist medical products it is essential that we have the best manufacturing partner on board. Our working partnership with them is very much on-going with the prospect of more new projects in the future.” Jason Smith, General Manager at Bedfont Scientific

The latest from ITL

News
ITL Group achieves double ISO 13485:2016 recertification

Global contract design and manufacturing partner, ITL Group (a G&H company) receives ISO 13485:2016 recertification for its Quality Management System (QMS) throughout its UK and US operations following a review by the British Standards Institute (BSI).

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Resource
Applying a regulatory approach – a guide for medical device startups

To ensure product quality and patient safety, medical device manufacturers must adhere to specific regulatory requirements and comply with rigorous safety standards. Are you aware of the regulatory approach necessary to compliantly manage your device from concept through to commercialisation?

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Case Study
Magnasense

From lab based analysis to mobile and disposable ‘point of care testing’ (POCT)

View this case study >