Increasing Operational Efficiency

INCREASING OPERATIONAL EFFICIENCY

With competitive pressure increasing, life science organizations are striving to improve time-to-market, whilst controlling operating costs.

This is leading the need to both streamline internal processes as well as remove any duplication of effort in processes, data and functions. Any paper-based processes may be intrinsically slow and subject to risk of errors.

Where systems or processes have been developed in local functions, there may be duplication of data or tasks, leading to repetition of effort, or more significantly, inconsistencies that lead to issues of quality or non- compliance.

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How we helped one of our clients with this challenge:

  • European Medical Device Manufacturer
  • Sought to reduce waste from IFU over-production
  • Implemented our print-on-demand solution
  • Single language IFUs now printed at time of shipment
  • Eliminating 175 tons of paper waste, saving $8M per annum.

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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INCREASING OPERATIONAL EFFICIENCY LABELING

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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