Tag: Manufacturing Deviations

Managing Deviations in Batch Records for Enteric-Coated Tablets

May 9, 2025 Admin

Managing Deviations in Batch Records for Enteric-Coated Tablets Managing Deviations in Batch Records for Enteric-Coated Tablets Introduction: In the pharmaceutical industry, maintaining the integrity of batch records is crucial for ensuring the quality and compliance of drug products. Enteric-coated tablets, designed to withstand the acidic environment of the stomach and dissolve in the more neutral…

Solid Dosage form, Tablets

Managing Documentation Deviations in Process Validation Protocols

May 7, 2025 Admin

Managing Documentation Deviations in Process Validation Protocols Managing Documentation Deviations in Process Validation Protocols Introduction: In the pharmaceutical industry, process validation is a critical component of ensuring product quality and compliance with regulatory standards. It involves a series of documented procedures and protocols designed to confirm that a manufacturing process consistently produces a product meeting…

Solid Dosage form, Tablets

Addressing Deviations in Process Validation for Sugar-Coated Tablets

March 11, 2025 Admin

Addressing Deviations in Process Validation for Sugar-Coated Tablets Addressing Deviations in Process Validation for Sugar-Coated Tablets Introduction: The pharmaceutical industry continuously strives for excellence in manufacturing practices, ensuring product quality and compliance with stringent regulations. Among various dosage forms, sugar-coated tablets remain a staple due to their ability to mask unpleasant tastes and enhance the…

Solid Dosage form, Tablets