In pharmaceutical industry, a non-conformance is any deviation from approved specifications, procedures, or regulatory requirements. It can affect product quality, safety, efficacy, or compliance. It signals that a process, product, or documentation has failed to meet...
Visual inspection in the pharmaceutical industry is a critical quality control step. Pharma visual inspection is a systematic examination of pharmaceutical products (often 100% of units) to identify visible defects before release. It is primarily applied to sterile...
Self-inspection in pharma companies is a planned, systematic internal audit process aimed to evaluate processes, facilities, and systems. It is designed to ensure compliance with Good Manufacturing Practices (GMP), regulatory requirements, and internal quality...
Blending has a vital role in the pharmaceutical industry, as drugs are manufactured by mixing various components. It is the process of thoroughly mixing all the ingredients. Additionally, the blending has to be performed at a particular temperature either in dry or...
Pharmaceutical industry technology transfer is vital to improve the quality of drugs available in the market. It is essential for drug discovery and development of new medicinal products. Herein, we have detailed what is technology transfer in pharmaceutical industry,...