Tag: Risk management in CSV

If you don’t find what you are looking for, try using a different term or contact us.

Software validation vs verification in GMP computerized systems with lifecycle and compliance focus

Software Validation vs Verification in GMP

Software validation vs verification explained under EU GMP Annex 11, FDA 21 CFR Part 11, and GAMP 5, with practical...
Featured image titled ‘What Is GAMP 5?’ showing a laboratory software engineer working at a computer with code on screen, used for an article explaining GAMP 5 risk-based validation, software categories, and regulatory alignment.

GAMP 5 in CSV: Definition, Categories, and Pharma Guidelines

Understand GAMP 5 with simple guidance on lifecycle control, validation deliverables, software categories, and risk-based decision-making in GMP environments....
Software Validation in GMP featured image with digital binary code and compliance theme.

Continuous Software Validation in GMP: Risk-Based Control Across the Lifecycle

Explore risk-based software validation in GMP, from CSV to continuous assurance, ensuring compliance, data integrity, and efficiency....
Quality Risk Management in Computer System Validation (CSV) featured image with digital compliance and validation icons.

Quality Risk Management in Computer System Validation (CSV)

Explore how risk management in CSV optimizes validation by focusing on critical functions, ensuring compliance and efficient use of resources....

BECOME A GMP INSIDER

Stay in touch and be the first to get the latest GMP News!