Data Integrity

Standard Operating Procedure (SOP) for Audit Trail Review

Standard Operating Procedure (SOP) for Audit Trail Review

Leave a Comment / Pharmaceutical Industry /
This comprehensive Standard Operating Procedure (SOP) for Audit Trail Review outlines the systematic process for reviewing electronic audit trails to ensure data integrity and compliance with regulatory standards. It details responsibilities, review procedures, documentation requirements, and training protocols for personnel involved in the audit trail review process. This SOP is essential for maintaining the accuracy, consistency, and reliability of electronic records within an organization.

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HPLC

Best Practices for Documentation in HPLC Method Development

Leave a Comment / HPLC /
Documenting the HPLC (High-Performance Liquid Chromatography) method development process is not only a good practice but also an essential requirement for ensuring the reproducibility, reliability, and compliance of analytical methods. In this article, we explore the best practices for documentation in HPLC method development, shedding light on the importance of comprehensive and organized records throughout

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HPLC Method Transfer and Validation: Ensuring Quality Assurance

Leave a Comment / HPLC /
High-Performance Liquid Chromatography (HPLC) is a widely used analytical technique in various industries, including pharmaceuticals, food, environmental monitoring, and more. Ensuring the consistency and reliability of HPLC methods when transferring them between laboratories or instruments is of paramount importance. In this article, we delve into the world of HPLC method transfer and validation, highlighting their

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