Tag: pharmaceutical guidelines

Addressing Coating Layer Delamination During Quality Testing

March 3, 2025 Admin

Addressing Coating Layer Delamination During Quality Testing Addressing Coating Layer Delamination During Quality Testing Introduction: Coating layer delamination in tablets is a critical issue in the pharmaceutical industry, impacting both product efficacy and patient safety. The coating on a tablet not only serves an aesthetic function but also plays a crucial role in controlling the…

Solid Dosage form, Tablets

Preventing Powder Loss During Compression in High-Speed Machines

March 2, 2025 Admin

Preventing Powder Loss During Compression in High-Speed Machines Preventing Powder Loss During Compression in High-Speed Machines Introduction: The pharmaceutical industry is renowned for its stringent quality standards, especially in the manufacturing of solid dosage forms like tablets. One critical aspect of tablet production is the compression process, which often faces the challenge of powder loss….

Solid Dosage form, Tablets

Validating Adequacy of Clean Steam Systems for Film-Coating Equipment

March 2, 2025 Admin

Validating Adequacy of Clean Steam Systems for Film-Coating Equipment Validating Adequacy of Clean Steam Systems for Film-Coating Equipment Introduction: In the pharmaceutical industry, ensuring the adequacy of clean steam systems is crucial for the successful operation of film-coating equipment used in tablet production. Clean steam, often used for sterilization and process control, must be free…

Solid Dosage form, Tablets

Validating Agglomeration Control Measures in Fluid Bed Granulation Processes

March 2, 2025 Admin

Validating Agglomeration Control Measures in Fluid Bed Granulation Processes Validating Agglomeration Control Measures in Fluid Bed Granulation Processes Introduction: In the pharmaceutical industry, the production of solid dosage forms such as tablets relies heavily on fluid bed granulation processes. This technique is essential for enhancing the flowability and compressibility of powders, which directly impacts the…

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

Ensuring Adequacy of Air Velocity Monitoring for Cleanroom HVAC Validation

March 1, 2025 Admin

Ensuring Adequacy of Air Velocity Monitoring for Cleanroom HVAC Validation Ensuring Adequacy of Air Velocity Monitoring for Cleanroom HVAC Validation Introduction: In the pharmaceutical industry, maintaining the integrity of cleanroom environments is critical to ensuring product quality and safety. Cleanrooms are controlled spaces where air quality, temperature, and humidity are carefully regulated to minimize contamination…

Solid Dosage form, Tablets

Validating Consistency in Cleanroom Pressure Differentials for Coated Tablet Production

March 1, 2025 Admin

Validating Consistency in Cleanroom Pressure Differentials for Coated Tablet Production Validating Consistency in Cleanroom Pressure Differentials for Coated Tablet Production Introduction: In the pharmaceutical industry, maintaining a sterile environment is crucial for the production of high-quality coated tablets. Cleanrooms are designed to minimize contamination and ensure product safety. One essential aspect of cleanroom functionality is…

Solid Dosage form, Tablets

Troubleshooting Failures in Compressed Air Filtration Systems for Multi-API Tablets

March 1, 2025 Admin

Troubleshooting Failures in Compressed Air Filtration Systems for Multi-API Tablets Troubleshooting Failures in Compressed Air Filtration Systems for Multi-API Tablets Introduction: In the pharmaceutical industry, the production of multi-API tablets involves complex processes where the purity and quality of compressed air play a crucial role. Compressed air is a critical utility in tablet manufacturing, influencing…

Solid Dosage form, Tablets

Controlling Humidity Variations in Compression Stages

March 1, 2025 Admin

Controlling Humidity Variations in Compression Stages Controlling Humidity Variations in Compression Stages Introduction: In the realm of pharmaceutical manufacturing, maintaining the integrity and quality of solid dosage forms is paramount. Among the various stages of tablet production, the compression stage stands out as a critical phase where humidity control plays a decisive role. Humidity variations…

Solid Dosage form, Tablets