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Follow on Google News | Datex Software Now Includes Features to Facilitate New FDA DQSA Regulation ComplianceBy: Datex Corporation Key provisions of the new FDA DQSA regulation include requirements for product identification, tracing and verification. All drug products are required to be encoded with a unique product identifier that must be at the smallest saleable unit and must be able to be verified at the package level standardized numerical identifier. Affected pharmaceutical industry supply chain businesses will benefit from using state-of-the- Datex Pharmaceutical Software enables full track and trace of serialized and Lot controlled products and provides a comprehensive audit trail and system validation. Datex software provides the ability to quarantine goods and enables multiple simultaneous holds. In addition, Datex Pharmaceutical Edition provides a full suite of QA/QC tools, handles both GS1 barcode processing and RFID and enables product recall tracking and enforcement process. Microsoft based Datex software is powered by workflow, configurable business processes that allow operations to make changes without altering system code. This enables customized business processes at a fraction of the cost of competitive software products and expedited implementation time. About Datex In successful operation since 1978, Datex has helped companies operate more efficiently and productively using state-of-the- For more information, please contact Laura Olson, Director of Sales and Marketing at 800.933.2839 ext.243 or via email at lolson@datexcorp.com. End
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