Verification vs Validation in QMS: Key Differences for Compliance
Quality Management Systems (QMS) in regulated industries, such as pharmaceuticals, biotechnology, and medical devices, rely on two critical yet frequently misunderstood processes: verification and validation. These concepts form the foundational pillars of robust QMS frameworks, ensuring that products are both built correctly and fit for their intended use. When organizations misinterpret or misuse these terms, […]
Continue reading