Category: Quality assurance

In the highly regulated pharmaceutical industry, every batch of medication or raw material must be tested rigorously for quality and purity. A Certificate of Analysis, or COA, is a document that encapsulates the results of this crucial testing, serving as a pillar of patient safety and regulatory compliance.

According to Good Manufacturing Practices (GMP), every batch of a drug product must have a comprehensive record. This critical document, known as the **Batch Production and Control Record (BPCR)**, ensures product quality, safety, and regulatory compliance throughout the manufacturing process.