TrackWise System – Master Data Management
Zamann Pharma Support provides specialized consultancy services for the management of Master Data within TrackWise, ensuring accuracy, consistency, and compliance with regulatory and operational requirements. Our approach includes the structuring, validation, and continuous maintenance of Master Data to optimize system performance and reliability.
By implementing strong governance practices, we help companies maintain data integrity and improve the efficiency of quality processes managed within TrackWise.
Master Data Structuring and Standardization
We analyze and define a structured approach for Master Data elements, such as suppliers, products, equipment, and processes, ensuring consistency across the TrackWise system. This includes standardizing naming conventions, categorizing data, and defining relationships between data elements to improve usability and reporting.
Data Accuracy and Integrity Verification
Our experts conduct periodic reviews and audits of existing Master Data records to identify inconsistencies, redundancies, or outdated information. We provide corrective action plans and update strategies to maintain compliance with GMP, FDA, and other regulatory requirements, ensuring data reliability for decision-making.
Ongoing Master Data Maintenance and Governance
We establish governance frameworks and maintenance routines to ensure continuous data accuracy. This includes defining ownership roles, implementing approval workflows for data changes, and training teams on best practices for maintaining high-quality Master Data in TrackWise.
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.
