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Life Science Software Validation

Our life science software validation is offered by our partner, CompliancePath, an end-to-end health and life science compliance services provider. Anyone operating in these sectors requiring validation can receive independent assurance that your software works in the way you need it to.

Request a consultation to discuss our software validation options.

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Business Benefits

Software validation is crucial within life sciences. It ensures that you are compliant with standards and regulations which require validation, such as ISO 13485 and Good Automated Manufacturing Practice (GAMP).

  • Improve Resilience

    A stable documented platform configured to your exact specifications.

  • Improve Resilience

    A tool that will perform consistently every time it is used.

  • Improve Resilience

    Verified user roles and security.

  • Improve Resilience

    Significant improvements in data quality and integrity.

  • Improve Resilience

    Decreased failure rates.

  • Improve Resilience

    Fewer recalls and corrective actions.

  • Improve Resilience

    Less risk to patients and users.

  • Improve Resilience

    Reduced liability to manufacturers.

Q-Pulse QMS software

Q-Pulse QMS Software Validation

Q-Pulse validation provides independent assurance of your QMS, allowing you to configure it to your internal processes and systems. It saves a considerable amount of internal resources and dedicated time, allowing you to get started with Q-Pulse as quickly as possible in a compliant manner.

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PleaseReview document co-authoring and review software

PleaseReview Software Validation

Our validation service for PleaseReview gives you assurance that the software works in the way you need it to, cutting down months of focus-intensive work to just 10 days. Your validation documents will also be updated when a new version of the software is released, ensuring you are always compliant.

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Q-Pulse QMS software

General Software Validation

CompliancePath offer validation expertise on software applications that impact a life science organisation under regulatory control. This could be any system ranging from an ERP to a LIMS platform which will deliver real business outcomes for customers.

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