This blog explores Analytical Method Validation (AMV) in the pharmaceutical industry, covering its stages and differentiating between verification and validation. It emphasizes the importance of AMV for ensuring accurate and reliable analytical methods. By following method development, qualification, and validation stages, pharmaceutical companies can maintain product quality and compliance.
In the realm of product manufacturing and quality control, the verification and validation process plays a crucial role. Three key components of this process are IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification). In this blog post, we will delve into the significance of each phase and how they contribute to ensuring product integrity and regulatory compliance.