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Siedlerstraße 7 | 68623 Lampertheim, Germany

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Labware LIMS – Continuous Validation Support

We provide Labware LIMS – Continuous Validation Support consultancy services to help companies maintain the validation status of their Labware LIMS system. This involves creating or reviewing validation documents, access and user roles evaluation, test execution, and performing comprehensive risk assessments. The service ensures alignment with GAMP5 guidelines and regulatory requirements, mitigating compliance risks and maintaining the system’s operational integrity over time

Labware LIMS – Continuous Validation Support

Validation Testing and Documentation

Performing comprehensive validation tests, including system functionality and performance tests, to verify that changes met predefined requirements. Creating or updated essential validation documents, such as test scripts, summary reports, and traceability matrices, to ensure compliance and audit readiness.

Access Permissions and User Role Evaluation

Conducting a detailed review of user access levels and roles to ensure compliance with data integrity and security requirements. Providing recommendations to improve role assignments and mitigate potential risks associated with unauthorized access.

Master Data Change Impact Assessments

Evaluating the impact of master data changes on the validation status, identifying risks and proposing corrective actions to ensure that the validation status of the system remains aligned with operational and regulatory expectations.

Tailored Solutions for Digital Transformation

Zamann Pharma Support offers customized digital solutions to streamline pharmaceutical operations. From AI-driven automation to robust platforms like eQMS and LIMS, we ensure seamless integration that enhances efficiency and compliance. Our expert team develops systems tailored to your specific business needs, ensuring optimal performance.

Why Zamann?

Zamann Pharma Support is a leader in delivering innovative digital solutions for the pharmaceutical industry. With extensive experience and specialized knowledge, we understand the unique challenges of digital transformation and regulatory compliance within a GMP framework. We support companies to turn paper based procedures to globally managed and fully digitized solution and have partnered with strong service providers for LMS, LIMS, QMS or Validation solutions.

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