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Zamann Pharma Support (ZPS) offers Ongoing Validation Support for the TrackWise System, ensuring that the software consistently meets regulatory compliance and operational requirements throughout its lifecycle. Our expert team provides comprehensive validation strategies customized to the specific needs of pharmaceutical organizations, enabling them to maintain high-quality standards in data integrity and system performance. We focus on delivering thorough documentation and systematic testing processes to support both initial validation and ongoing compliance efforts.
ZPS collaborates with clients to develop a detailed validation plan that outlines the scope, objectives, and methodologies for validating the TrackWise System. This includes defining the specific regulatory requirements that must be met and establishing timelines and resource allocations for the validation process.
Our team conducts rigorous testing to validate system functionalities, including installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). This ensures that the TrackWise System operates as intended and meets all predefined acceptance criteria, with detailed documentation maintained throughout the process.
ZPS prepares and reviews all necessary validation documentation, including test plans, protocols, and final reports, to ensure compliance with industry standards and regulatory guidelines. We also conduct regular compliance audits and provide guidance on best practices, helping clients maintain their validation status and address any gaps or non-conformities that may arise over time.
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.
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.
