Tag: Computer System Validation (CSV)

How to Handle Software Updates and Revalidation

How to Handle Software Updates and Revalidation How to Handle Software Updates and Revalidation In the rapidly evolving landscape of the pharmaceutical industry, ensuring compliance with regulatory requirements while managing software updates and revalidation has become a critical focus for…

Validating Data Transfers in Software Systems

Validating Data Transfers in Software Systems Validating Data Transfers in Software Systems Validating data transfers in software systems is a crucial aspect of ensuring compliance and integrity in the pharmaceutical industry. This step-by-step tutorial outlines the validation lifecycle, detailing essential…

How to Perform Version Control for Spreadsheets

How to Perform Version Control for Spreadsheets How to Perform Version Control for Spreadsheets In the pharmaceutical industry, computer system validation (CSV) is an essential process to ensure that computerized systems adhere to regulatory requirements and support the safe and…

User Acceptance Testing (UAT) in Pharma CSV

User Acceptance Testing (UAT) in Pharma CSV User Acceptance Testing (UAT) in Pharma CSV User Acceptance Testing (UAT) is a critical phase in the computer system validation (CSV) lifecycle in the pharmaceutical industry. This tutorial provides a detailed, step-by-step guide…

Compliance Requirements for Custom Software in GMP Use

Compliance Requirements for Custom Software in GMP Use Compliance Requirements for Custom Software in GMP Use The implementation of custom software in the pharmaceutical industry demands rigorous adherence to compliance requirements to ensure product quality and patient safety. This article…

Spreadsheet Validation Protocol Sample for Audit Readiness

Spreadsheet Validation Protocol Sample for Audit Readiness Spreadsheet Validation Protocol Sample for Audit Readiness In the highly regulated pharmaceutical industry, ensuring compliance with validation requirements is vital for maintaining product quality and safety. With the implementation of regulations such as…

IQ/OQ for Software Systems: What Needs to Be Documented

IQ/OQ for Software Systems: What Needs to Be Documented IQ/OQ for Software Systems: What Needs to Be Documented In the highly regulated pharmaceutical and biotechnology industries, ensuring compliance through rigorous validation procedures is paramount. This article provides an in-depth, step-by-step…

Macro and Formula Locking Techniques for GMP Spreadsheets

Macro and Formula Locking Techniques for GMP Spreadsheets Macro and Formula Locking Techniques for GMP Spreadsheets In the realm of pharmaceutical manufacturing and quality control, ensuring data integrity and compliance is paramount. Effective gxp validation plays a critical role in…

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…

Spreadsheet Inventory and Risk Assessment Template

Spreadsheet Inventory and Risk Assessment Template Spreadsheet Inventory and Risk Assessment Template This article provides a comprehensive step-by-step tutorial on implementing a spreadsheet inventory and risk assessment within the context of kneat validation. This approach aligns with regulatory frameworks, including…