We work with these teams

WE WORK WITH THESE TEAMS

Choosing the right labeling solution is not easy. It needs to help achieving regulatory compliance; be efficient; help overcoming technical challenges, be user friendly; reduce various types of risks and assist with expansion or consolidation.

Different teams within a business have different requirements. An end-to-end labeling solution needs to fulfil all these requirements and assist all the teams in their objectives.

In our 20 years’ experience in life sciences, we learned that all these teams are equally important and we need to discuss individual needs and expectations from early phases.

“Once PRISYM ID clearly understood our requirements they identified a solution that integrated with numerous existing systems and processes, eliminated many areas of concern and delivered improved label printing efficiency, accuracy and quality.”

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LATEST RESOURCES

EU MDR Labeling – ‘Touch Your Label Once’ Strategy EU MDR Labeling – ‘Touch Your Label Once’ Strategy Posted in: Achieving Regulatory Compliance, Assisting with Consolidation, Business Analysis, Increasing Operational Efficiency, Information Technology, Medical Device, Operations & Labeling, Overcoming Technical Challenges, Project Managers, Reducing Risks, Regulatory & Compliance, Supply Chain, Webinar -

Join PRISYM ID for this free webinar to learn how an effective “touch your label once” strategy for EU MDR labeling can streamline processes and reduce the cost of a global label change.

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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, Business Analysis, Increasing Operational Efficiency, 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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