Tag: Quality assurance

Did you know that a single batch of medicine can contain millions of tablets, making batch-by-batch testing impractical? This is why understanding **what is GMP in pharmacology** is crucial, as it mandates a system of controls to ensure quality is built into every step of the manufacturing process, from raw materials to final product.

Under Title 21 of the Code of Federal Regulations (CFR), pharmaceutical manufacturers must maintain meticulous records for every drug batch produced [1.3.2, 1.3.3]. Central to this is understanding: **what is BPCR in pharma?** It stands for the Batch Production and Control Record, a cornerstone of quality and regulatory adherence.

According to the EU GMP Guide Part I, a CoA provides an overview of test results for a product batch. **What is CoA in pharma?** It's a formal document issued during drug manufacturing and development to confirm that a specific batch of a product meets its pre-established quality specifications.

The global pharmaceutical market is projected to reach over $1.7 trillion by the end of 2025, fueling significant career opportunities [1.8.2]. When considering a career path, it's crucial to ask: **which department is best in the pharma industry** for long-term success and satisfaction?