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Tag: GMP in Pharmaceuticals

Ensuring Adherence to GMP Standards in Documentation for QA Processes

Posted on March 20, 2025 By Admin

Ensuring Adherence to GMP Standards in Documentation for QA Processes Ensuring Adherence to GMP Standards in Documentation for QA Processes Introduction: In the world of pharmaceutical manufacturing, ensuring the quality and safety of products is paramount. This is where Good Manufacturing Practice (GMP) standards come into play, serving as a cornerstone for quality assurance (QA)…

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Solid Dosage form, Tablets

Troubleshooting Failures in Content Uniformity Tests for Film-Coated Tablets

Posted on March 20, 2025 By Admin

Troubleshooting Failures in Content Uniformity Tests for Film-Coated Tablets Troubleshooting Failures in Content Uniformity Tests for Film-Coated Tablets Introduction: Content uniformity is a critical quality attribute in the manufacturing of film-coated tablets. Ensuring that each tablet contains the appropriate amount of active pharmaceutical ingredient (API) is essential for efficacy, safety, and regulatory compliance. Content uniformity…

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Solid Dosage form, Tablets

Managing Failures in Steam Quality Validation for Enteric-Coated Tablet Equipment

Posted on March 4, 2025 By Admin

Managing Failures in Steam Quality Validation for Enteric-Coated Tablet Equipment Managing Failures in Steam Quality Validation for Enteric-Coated Tablet Equipment Introduction: In the pharmaceutical industry, ensuring the sterility and quality of equipment used in the manufacturing process is critical, especially for enteric-coated tablets. Steam quality validation is a vital component of this quality assurance process….

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Solid Dosage form, Tablets
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