Tag: validation documentation

How to Investigate Data Discrepancies in Validation Logs

How to Investigate Data Discrepancies in Validation Logs How to Investigate Data Discrepancies in Validation Logs The integrity of data generated from computer systems in the pharmaceutical industry is paramount for compliance with regulatory guidelines. Data discrepancies can lead to…

Using Metadata to Ensure ALCOA+ Principles

Using Metadata to Ensure ALCOA+ Principles Using Metadata to Ensure ALCOA+ Principles In the pharmaceutical industry, ensuring data integrity is paramount for compliance with regulatory expectations and maintaining product quality. The ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, and the…

Data Integrity Training for Validation and QA Teams

Data Integrity Training for Validation and QA Teams Data Integrity Training for Validation and QA Teams Data integrity is a cornerstone of quality assurance in the pharmaceutical industry. As organizations implement computer systems for compliance with Good Manufacturing Practices (GMP),…

Backup and Recovery Requirements for Validation Files

Backup and Recovery Requirements for Validation Files Backup and Recovery Requirements for Validation Files In the realm of computer system validation in the pharmaceutical industry, the integrity and recoverability of validation files are paramount. These files constitute vital documentation that…

Validating Electronic Systems for Storing Validation Documents

Validating Electronic Systems for Storing Validation Documents Validating Electronic Systems for Storing Validation Documents In the pharmaceutical industry, effective computer system validation (CSV) is integral to ensure compliance with regulatory expectations and maintain data integrity. This article outlines a comprehensive…

Common Data Integrity Gaps Found in Validation Files

Common Data Integrity Gaps Found in Validation Files Common Data Integrity Gaps Found in Validation Files In the pharmaceutical industry, ensuring the integrity and compliance of validation documentation is critical. This article will guide you through a structured step-by-step validation…

Audit Trail Requirements for Validation Protocols and Reports

Audit Trail Requirements for Validation Protocols and Reports Audit Trail Requirements for Validation Protocols and Reports Step 1: Understanding User Requirements Specifications (URS) and Risk Assessment In the context of analytical method validation, the first step in the validation lifecycle…

Review and Approval Logs: Ensuring Attributable and Contemporaneous Entries

Review and Approval Logs: Ensuring Attributable and Contemporaneous Entries Review and Approval Logs: Ensuring Attributable and Contemporaneous Entries In the realm of pharmaceutical validation, the integrity of documentation is paramount. Review and approval logs play a critical role in ensuring…

Electronic vs Paper-Based Validation Documentation: Pros & Cons

Electronic vs Paper-Based Validation Documentation: Pros & Cons Electronic vs Paper-Based Validation Documentation: Pros & Cons 1. Understanding the Basics of System Validation System validation is a critical aspect of the pharmaceutical industry, ensuring that all systems used in the…

Handling Raw Data for Validation in Audit-Ready Format

Handling Raw Data for Validation in Audit-Ready Format Handling Raw Data for Validation in Audit-Ready Format The validation of pharmaceutical processes is both a regulatory requirement and a crucial aspect of maintaining product quality. One of the key areas within…