Sectors

SECTORS

Companies within the Medical Devices, Pharmaceuticals and Clinical Trials 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.”

WE OPERATE IN THESE SECTORS

Medical Devices icon - Sectors

MEDICAL DEVICES

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

CLINICAL TRIALS

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

PHARMACEUTICALS

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

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LATEST RESOURCES

EU MDR infographic - EU MDR – Is the Industry Planning for It? Are You? EU MDR – Is the Industry Planning for It? Are You? Posted in: Achieving Regulatory Compliance, Business Analysis, Infographic, Information Technology, Medical Device, Operations & Labeling, Project Managers, Regulatory & Compliance, Supply Chain -

Whether you’re producing medical devices within Europe or supplying to Europe from the rest of the world, as a manufacturer or supplier, you will need to adhere to the EU MDR by May 2020.

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