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The Latest in Data Integrity Best Practices

The Latest in Data Integrity Best Practices

Maintaining data integrity in current good manufacturing practice (CGMP) environments is crucial to ensuring the safety, efficacy and quality of drugs. Unprotected data can present a risk to business continuity, result in costly product recall or even lead to a breakdown of public and regulator trust.

Understanding how data integrity workflows and best practices are defined can help researchers to establish a secure and compliant environment.

This whitepaper explores the importance of data integrity in drug manufacturing workflows. It highlights key resources that can help you stay up to date with the latest regulations.

Download this whitepaper to discover:

  • The role of integrity measures in data traceability, accuracy and reliability
  • Useful system access approaches, audit trails and electronic signatures
  • Key compliance requirements according to CFR and European Union law

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