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.

Utilizing the latest technologies and standards, PRISYM 360 - The Only Labeling Solution Dedicated to Life Science -  also offers flexibility in deployment options, including On Premise, Private Cloud and SaaS models, ensuring it can integrate fully with enterprise IT strategies and policies.

“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…

Read More

Clinical Trials icon - Sectors


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

Read More

Pharmaceuticals - Sectors


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

Read More



This solution provides organizations with complete label integrity to meet the strictest compliance requirements for FDA & EU regulations, specifically FDA 21 CFR Parts 11, 810, and 820.

Read More


This solution enables organizations to address the challenges of complying with FDA and other regulations by delivering access to a compliance ready platform in the Cloud.

Read More


Our team of in-house compliance and validation subject matter experts and professional services and support teams can help you from implementation through to delivery and beyond.

Read More


Biotec webinar - Are you ready for the Annex VI EU No 536/2014 labeling changes? Are you ready for the Annex VI EU No 536/2014 labeling changes? Posted in: Business Analysis, Clinical Trials, Increasing The Operational Efficiency, Information Technology, Operations & Labeling, Overcoming The Technical Challenges, Project Managers, Supply Chain, Webinar -

Are your current packaging and labeling processes preventing you from creating a faster, more flexible supply chain?

Are you struggling to implement an on-demand packaging model...

Read More
PRISYM ID Recalls E-book How to Avoid Four Common Labeling Product Recalls Posted in: Achieving Regulatory Compliance, Increasing The Operational Efficiency, Medical Device, Operations & Labeling, Project Managers, Regulatory & Compliance, Whitepaper -

Companies’ continued reliance on manual processes and disparate labeling systems often culminates in pricey product recalls.

Read More