Pharmaceutical quality control is a crucial component of drug manufacturing and regulatory compliance, ensuring that medications are consistently safe, effective, and free from harmful impurities.
Quality control processes evaluate raw materials, active pharmaceutical ingredients, excipients, intermediate compounds, and the final dosage forms used by patients. Laboratories conduct rigorous physical, chemical, microbiological, and analytical tests to confirm that products meet established standards. These assessments include potency verification, purity analysis, dissolution testing, stability evaluation, and physical consistency checks. Any deviation from defined specifications can impact therapeutic performance or pose health risks, making strict QC protocols essential throughout production.
The global pharmaceutical industry adheres to high regulatory standards established by authorities such as the FDA, EMA, WHO, and regional health agencies. Good Manufacturing Practices (GMP) guide the entire lifecycle of drug production, from material sourcing to packaging and distribution. Quality control laboratories apply advanced technologies such as high-performance liquid chromatography, mass spectrometry, spectroscopy,…
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