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    Maintain GDP compliance and ensure supply chain integrity

    Ensure your products meet regulatory requirements and reach patients safely and effectively by adhering to Good Distribution Practices (GDP) guidelines.
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    • yusen logistics
    • Livlina
    • Distrilog
    • Hospital Logistics
    • ODT

    The key components of GDP controlled in one space

    Image that represents the main challenges of not having a GMP-compliant QMS | Scilife

    Challenge

    Maintaining the quality of medicinal products, APIs, and excipients demands precise documentation, strict controls, and strong risk management.

    However, many companies struggle to implement a QMS that meets Good Distribution Practice (GDP) standards.  The result? Gaps in compliance, increased risk, and operational inefficiencies.

    Image that represents the benefits of implementing Scilife GMP-Compliant QMS | Scilife

    Solution

    Why stay in the dark when Scilife’s eQMS can light the way? Our GDP-compliant solution sharpens quality and data integrity across your supply chain.

    Ensure GDP compliance by efficiently managing documentation, tracking quality events in real-time, automating compliance tasks, customizing workflows for CAPAs and much more!

    Icon that represents how to improve your Quality Control with Scilife GMP-Compliant QMS | Scilife

    Ensure data integrity and GDP compliance

    Maintain accurate, reliable data through validation processes and automated compliance checks.
    Make your pharma supply chain agile

    Make your pharma supply chain agile

    Leverage real-time visibility and streamlined workflows to enable rapid adjustments and improve coordination.
    Accelerate time to market

    Accelerate time to market

    Launch your product faster by optimizing quality assurance processes and minimizing delays.
    Icon that represents how Scilife GMP-Compliant improves efficiency | Scilife

    Achieve cost and time savings

    Cut down on manual labor, minimize errors, and streamline workflows through digitization and automation.

    Be GDP compliant and adhere to FDA 21 part 11 regulations


    Our QMS software will allow you to:

    • Manage various document types, automate version control, and ensure compliance with electronic signature regulations.
    • Use customizable electronic forms to document processes, ensuring consistency, compliance, and traceability according to ALCOA principles.
    • Ensure data integrity by controlling the use of manual forms with unique identifiers and tracking printed documents through unique barcodes.
    FDA 21 CFR Part 11 | Scilife

    Navigate deviations and nonconformities during distribution


    Our QMS software will allow you to:

    • Create your quality event instantly on any device to reduce the risk of forgetting or missing an important quality event.
    • Capture and manage any type of quality event in real-time.
    • Link quality events to investigations, assessments, and CAPAs needed to mitigate future risks.
    Navigate deviations | Scilife

    Build strong alliances with your suppliers


    Our QMS software will allow you to:

    • Implement a clear and standardized procedure for qualifying and auditing suppliers, distributors, and logistics providers.
    • Qualify or reject suppliers using a simple and compliant workflow aligned with the best GDP guidelines.
    • Execute thorough Risk Assessments in accordance with ICH Q9 guidelines as part of the qualification process.
    Build strong alliances | Scilife

    Empower your workforce


    Our QMS software will allow you to:

    • Ensure all employees receive adequate training and comply with cGMP regulations.
    • Streamline the management of both initial and ongoing employee training through automation.
    • Gain a clear overview of training processes and compliance maintain detailed records of their progress.
    Empower your workforce | Scilife

    "For most employees it took about 6 to 8 weeks to get used to Scilife so for the majority, the transition was very easy. There were a few that found it a bit more challenging which is normal considering a change like this is always hard. This number would have been much higher if we had opted for a more complex solution."


    Astrid Thorissen Astrid Thorissen,
    Global Healthcare Quality Manager at Yusen Logistics

    comillas
    Illustration that represents how Scilife smart QMS can help you improve your quality processes

    Turn quality into your brightest asset with Scilife

    When we embrace quality, brilliant things happen!

    Book a Demo

    EMEA Office
    Louizalaan 489
    1050 Brussels
    Belgium

    US Office
    Scilife Inc.
    228 E 45th St. RM 9E
    New York, NY 10017

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      EMEA Office
      Louizalaan 489
      1050 Brussels
      Belgium

      US Office
      Scilife Inc.
      228 E 45th St. RM 9E
      New York, NY 10017

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