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Siedlerstraße 7 | 68623 Lampertheim, Germany

info@zamann-pharma.com

TrackWise System – Version Upgrade Support

We provide expert consultancy for companies upgrading their TrackWise system version, ensuring a seamless transition without disruptions to operations or compliance risks. Our service includes a comprehensive impact assessment, validation strategy, and user support to maintain system integrity and alignment with regulatory requirements. By implementing structured upgrade processes, we help organizations optimize system performance while minimizing downtime and ensuring user adoption.

Impact Assessment and Upgrade Planning

We conduct a thorough evaluation of the existing TrackWise configuration, identifying potential risks, system dependencies, and business process impacts. A detailed upgrade plan is developed, including timelines, resource allocation, and mitigation strategies to ensure a smooth transition.

Validation and Compliance Assurance

Our experts manage the validation activities required for the upgraded version, including test script creation, execution of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), and risk assessments to comply with GAMP5, FDA, and other global regulatory standards.

User Training and Post-Upgrade Support

To ensure a successful upgrade, we provide training sessions for end-users and administrators, focusing on new functionalities, process changes,
and best practices. Additionally, we offer postupgrade monitoring and troubleshooting support to quickly address any issues and optimize system
performance.

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.

Modern Laboratory Work Space

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