Companies within the medical device, clinical trials and pharmaceuticals sectors are amongst those that PRISYM ID has fostered the most successful working relationships with, partnerships underpinned by industry-specific knowledge and expertise.

Our focus on life sciences industries enables us to provide you with the level of research and development needed to help you get ahead of your competition and lead the way in labeling quality and control.

We combine our industry specialism of regulatory requirements - such as FDA or EU compliance - with a partnership approach to product development and configuration.

Our configurable applications - designed in conjunction with industry leaders and customer user groups including Boston Scientific, Zimmer, Stryker, GSK, Pfizer, and Bristol Meyers Squibb - address both today’s challenges and tomorrow’s business needs.

“We have been working with PRISYM ID for some time now and have an excellent relationship. The solution provided by PRISYM ID makes a real difference in terms of efficiency and time saving, making our operators' jobs much easier.

PRISYM ID has made such a fundamental difference to our business. Due to the success of our deployment, we will be rolling out PRISYM ID’s labeling solution across other units as well. PRISYM ID will become our corporate partner for enterprise-wide labeling requirements.”


Medical Devices icon - Sectors


Global medical device organizations such as Boston Scientific, Zimmer, and Stryker have successfully adopted lifecycle label management solutions…

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Clinical Trials icon - Sectors


In designing an effective on-demand supply chain, it is the clinical trial
labeling that can present the most challenges…

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Pharmaceuticals - Sectors


Ever-changing regulatory statements, language translations and patient-led design considerations can all impact your timescales for producing….

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SaaS Demo PRISYM SaaS Demo: Validated Labeling for Small-to-Medium Medical Device Manufacturers Posted in: Medical Device, Webinar -

Join us for our demo to see how our validated labeling solutions have been helping organizations to achieve regulatory compliance, and increase their operational efficiency, reducing costs and the risk of recalls.

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PRISYM ID 10 Steps to EU MDR Labeling Implementation Guide 10 Steps to EU MDR Labeling Implementation Posted in: Achieving Regulatory Compliance, Medical Device, Operations & Labeling, Project Managers, Regulatory & Compliance, Whitepaper -

Whether you’re producing medical devices within Europe or supplying to Europe, as a manufacturer or supplier, you will need to adhere to the new EU MDR.

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