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Ensuring Data Integrity in the Pharma Space

Ensuring Data Integrity in the Pharma Space

Compliance with good manufacturing or laboratory practice (GMP or GLP) guidelines can help labs ensure the quality and integrity of biopharmaceutical data.


Poor data management or deliberate falsification can cause integrity breaches, undermine product quality and even result in costly recall events.


While a reliance upon manual and paper-based processes can introduce critical errors, electronic systems offer user-friendly, efficient solutions that can keep your data safe. 


This whitepaper explores advanced electronic solutions to streamline your biopharmaceutical workflow and help you stay compliant with the latest regulations.


Download this whitepaper to discover:

• The latest GLP and GMP compliant data management practices
• Common vulnerabilities in data management processes according to ALCOA+ principles
• A laboratory information management system (LIMS) that integrates notebook and execution system workflows
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