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Paperless Validation for Contract Research Organizations

ValGenesis helps you enforce an approved validation plan and related procedures so you can be audit-ready without preparation.

ValGenesis products replace inefficient paper-based validation processes with a 100% paperless, electronic system. ValGenesis will help your company save up to 50% in both time and budgetary costs across your validation process.

With multiple sites and employees distributed across locations maintaining unconnected paper-based quality systems, contract development and manufacturing organizations (CDMO and CMO) face several key challenges:

  • Wasted time and effort to manage and complete paper-based validation activities
  • Delayed communication and inconsistent standards
  • Risk of regulatory deviations and costly investigations

Furthermore, lack of integration can create islands of information that do not provide a holistic view of the validated state of systems. Integrated quality systems, together with validation processes, expedites critical compliance tasks and provides a complete history and traceability of a system’s validated state, as well as maintains robust data integrity control.

ValGenesis products are ideally suited for CDMOs and CMOs.

Now you can replace inefficient paper-based validation processes with a 100% paperless, electronic system that drives 50% reductions in both time and budgetary costs. Our unique technology manages an entire validation process from end to end, providing dynamic real-time validation status tracking, streamlining processes, improving communications between stakeholders, and ensuring/enforcing compliance and consistency throughout corporate validation processes.

  • Remove paper from your validation process
  • Consolidate information from distributed teams and processes
  • Enforce all regulatory compliance standards
  • Reduce the risk of investigations
Industry - Contract-Organizations
ValGenesis replaces inefficient paper-based validation processes with a 100% paperless, electronic system that drives 50% reductions in both time and budgetary costs.
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Event Presentation

Apply Quality by Design (QbD) for all Validation Types - QbD for All

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White Paper

ValGenesis VLMS Compliance Assessment - FDA 21 CFR Part II

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Ready to learn more about going paperless in your company?

Reach out to schedule a free, personal demo of the ValGenesis VLMS. We’ll show you our product in-depth and share our experience to identify the perfect solution for your organization.

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