A supplier audit in pharma is a formal evaluation of vendors providing raw materials, packaging, or services. The aim is to ensure they comply with Good Manufacturing Practices (GMP), regulatory standards, and quality expectations. It is a critical part of...
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...
Operational qualification has a vital role in ensuring high-quality products are being consistently manufactured. It is the third stage in the equipment qualification process. Operational qualification in pharmaceutical industry validates all equipment and sub systems...
The CDSCO has now opened the portal for Revised Schedule M deadline extension application. Revised Schedule M deadline extension will be applicable only for small and medium scale businesses having a turnover of less than 250 crore. We have prepared a detailed guide...
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