Project Managers

IS YOUR ROLE PROJECT MANAGEMENT?

When having to implement labeling software and label management systems to meet validation and compliance requirements, a Project Manager needs an industry recognized, intelligent solution.

It needs to be a product that is focused on efficiency, ensuring regulatory and legal compliance, improves timeframes and budgetary considerations, and supported by a reliable and market-leading company throughout the implementation process.

We understand that to manage a project successfully you need your team and your systems to be efficient and aligned so that expectations can be set, managed and achieved. We are confident that we exceed the quality, experience and services of any other solution provider, helping you to smoothly manage the implementation and integration of our labeling solution with your ERP/PLM systems on time and within the budget.

“PRISYM ID delivered on time as promised, despite an aggressive timeline, it wasn't just a sales pitch. They managed the project well working closely with our internal team. I would definitely work with them again“

CHOSEN BY THESE CUSTOMERS...

OFFERING THESE PRODUCTS AND SERVICES...

PRISYM 360

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.

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PRISYM SaaS

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.

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SERVICES

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

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PROJECT MANAGEMENT LABELING RESOURCES

EU MDR EU MDR’s Impact on Labeling: UDI in Europe and Other Changes Posted in: Achieving Regulatory Compliance, Business Analysis, Increasing Operational Efficiency, Medical Device, Operations & Labeling, Project Managers, Reducing Risks, Regulatory & Compliance, Supply Chain, Webinar -

Join medical device labeling and data experts from PRISYM ID and Reed Tech to learn about what the EU Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR) mean for labels in this free webinar.

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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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