Tag: pharmaceutical compliance

Validating Residual Solvent Control Measures in Coated Tablets

March 2, 2025 Admin

Validating Residual Solvent Control Measures in Coated Tablets Validating Residual Solvent Control Measures in Coated Tablets Introduction: Residual solvents are volatile chemicals used or produced in the manufacture of pharmaceutical substances, excipients, or in the preparation of drug products. Their presence in pharmaceuticals is a critical quality and safety concern, especially in coated tablets where…

Solid Dosage form, Tablets

Resolving Weight Variation Failures in Bilayer Tablets

March 2, 2025 Admin

Resolving Weight Variation Failures in Bilayer Tablets Resolving Weight Variation Failures in Bilayer Tablets Introduction: In the pharmaceutical industry, bilayer tablets have emerged as a sophisticated solution for delivering multiple drugs or achieving different release profiles in a single dosage form. However, maintaining uniform weight across these tablets poses significant challenges, impacting quality and efficacy….

Solid Dosage form, Tablets

Ensuring Adequacy of Water Flow in Purified Water Systems for Multi-Layer Tablets

March 2, 2025 Admin

Ensuring Adequacy of Water Flow in Purified Water Systems for Multi-Layer Tablets Ensuring Adequacy of Water Flow in Purified Water Systems for Multi-Layer Tablets Introduction: In the pharmaceutical industry, the production of multi-layer tablets demands meticulous attention to detail and stringent adherence to quality standards. One crucial aspect of this process is ensuring the adequacy…

Solid Dosage form, Tablets

Ensuring Robustness of Packaging for Tablets in Extreme Environmental Conditions

March 2, 2025 Admin

Ensuring Robustness of Packaging for Tablets in Extreme Environmental Conditions Ensuring Robustness of Packaging for Tablets in Extreme Environmental Conditions Introduction: In the pharmaceutical industry, the packaging of tablets plays a critical role in ensuring drug efficacy, safety, and shelf-life. For tablets distributed globally, packaging must withstand extreme environmental conditions such as high humidity, temperature…

Solid Dosage form, Tablets

Managing Over-Lubrication in Blending Processes for Compression

March 2, 2025 Admin

Managing Over-Lubrication in Blending Processes for Compression Managing Over-Lubrication in Blending Processes for Compression Introduction: In the realm of pharmaceutical manufacturing, ensuring the quality and efficacy of solid dosage forms like tablets is paramount. The blending process, a critical step in tablet production, often involves the use of lubricants to improve the flow of powder…

Solid Dosage form, Tablets

Addressing Non-Compliance in Stability Testing for Coated Tablets

March 1, 2025 Admin

Addressing Non-Compliance in Stability Testing for Coated Tablets Addressing Non-Compliance in Stability Testing for Coated Tablets Introduction: Stability testing is a critical component in the pharmaceutical industry, ensuring that drugs maintain their efficacy, safety, and quality over time. For coated tablets, this becomes even more crucial due to the additional complexity introduced by the coating…

Solid Dosage form, Tablets

Addressing Calibration Failures in Temperature Sensors for Utility Validation

March 1, 2025 Admin

Addressing Calibration Failures in Temperature Sensors for Utility Validation Addressing Calibration Failures in Temperature Sensors for Utility Validation Introduction: In the pharmaceutical industry, maintaining precise environmental conditions is crucial for ensuring product efficacy and safety. Temperature sensors play a vital role in utility validation, monitoring, and controlling critical processes. Calibration failures in these sensors can…

Solid Dosage form, Tablets