Tag: system validation

Risk Assessment for Minor vs Major Temperature Excursions

Risk Assessment for Minor vs Major Temperature Excursions Risk Assessment for Minor vs Major Temperature Excursions The pharmaceutical industry is bound by rigorous regulatory expectations concerning the integrity and efficacy of products during transport and storage. Effective system validation processes…

Coding Equipment Qualification: IQ/OQ/PQ Protocols

Coding Equipment Qualification: IQ/OQ/PQ Protocols Coding Equipment Qualification: IQ/OQ/PQ Protocols In the pharmaceutical and biologics sectors, ensuring that coding equipment operates within defined specifications is critical for compliance with Good Manufacturing Practices (GMP) and other regulatory frameworks. This comprehensive guide…

Airflow Directionality Testing: Qualitative and Quantitative Methods

Airflow Directionality Testing: Qualitative and Quantitative Methods Airflow Directionality Testing: Qualitative and Quantitative Methods In the pharmaceutical and biotechnology industries, the validation of systems employed in cleanrooms and controlled environments is a critical aspect of ensuring product quality and compliance…

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…

How Inspectors Review and Use Your VMP During Audits

How Inspectors Review and Use Your VMP During Audits How Inspectors Review and Use Your VMP During Audits In the pharmaceutical industry, the role of a Validation Master Plan (VMP) is crucial in ensuring compliance with regulatory requirements. This guide…

Validation of Off-the-Shelf Software in GxP Systems

Validation of Off-the-Shelf Software in GxP Systems Validation of Off-the-Shelf Software in GxP Systems In today’s regulated environments, the validation of off-the-shelf software in Good Practice (GxP) systems is crucial for compliance and maintaining data integrity. This article serves as…

Documenting In-Process Changes in Qualification Reports

Documenting In-Process Changes in Qualification Reports Documenting In-Process Changes in Qualification Reports In the complex landscape of pharmaceutical validation, the ability to navigate through the validation lifecycle with precision and attention to regulatory requirements is essential. This article serves as…

Common Mistakes in Writing Validation Protocols

Common Mistakes in Writing Validation Protocols Common Mistakes in Writing Validation Protocols In the pharmaceutical industry, the integrity of systems, processes, and documentation is paramount to ensuring product quality and compliance. This article provides a comprehensive, step-by-step guide geared towards…