Tag: manufacturing process

Managing Hardness Variability in High-Speed Compression Tablets

March 20, 2025 Admin

Managing Hardness Variability in High-Speed Compression Tablets Managing Hardness Variability in High-Speed Compression Tablets Introduction: In the pharmaceutical industry, tablets are a widely used solid dosage form, offering convenience in administration and precise dosing. However, ensuring the consistency of tablet hardness, especially during high-speed compression, is a critical quality attribute that directly impacts the dissolution…

Solid Dosage form, Tablets

Addressing Overheating Issues in HVAC Systems for High-Volume Tablet Production

March 17, 2025 Admin

Addressing Overheating Issues in HVAC Systems for High-Volume Tablet Production Addressing Overheating Issues in HVAC Systems for High-Volume Tablet Production Introduction: In the pharmaceutical industry, maintaining optimal environmental conditions is crucial for the manufacturing of solid dosage forms, particularly tablets. HVAC (Heating, Ventilation, and Air Conditioning) systems play a vital role in regulating temperature and…

Solid Dosage form, Tablets

Ensuring Compliance with GMP Standards During Validation of Compression Equipment

March 16, 2025 Admin

Ensuring Compliance with GMP Standards During Validation of Compression Equipment Ensuring Compliance with GMP Standards During Validation of Compression Equipment Introduction: In the pharmaceutical industry, compliance with Good Manufacturing Practice (GMP) standards is paramount to ensure the safety and efficacy of drug products. The validation of compression equipment, an essential process in tablet production, is…

Solid Dosage form, Tablets

Poor standardization of capsule defect classification criteria.

March 13, 2025 Admin

Poor standardization of capsule defect classification criteria. Poor standardization of capsule defect classification criteria. Introduction: In the pharmaceutical industry, capsules serve as a popular solid oral dosage form due to their ease of administration and ability to encapsulate a wide range of active pharmaceutical ingredients. However, the lack of standardized criteria for classifying capsule defects…

Capsules (Hard & Soft Gelatin), Solid Oral Dosage Forms

Addressing Residual Solvent Levels in Coated Tablets During In-Process Control

March 12, 2025 Admin

Addressing Residual Solvent Levels in Coated Tablets During In-Process Control Addressing Residual Solvent Levels in Coated Tablets During In-Process Control Introduction: The pharmaceutical industry is governed by stringent regulations to ensure the safety, efficacy, and quality of products. One critical aspect of manufacturing coated tablets is managing residual solvent levels during in-process control. Residual solvents…

Solid Dosage form, Tablets

Managing Failures in Stress Testing for Controlled Release Tablets

March 12, 2025 Admin

Managing Failures in Stress Testing for Controlled Release Tablets Managing Failures in Stress Testing for Controlled Release Tablets Introduction: In the pharmaceutical industry, controlled release tablets play a pivotal role in ensuring the precise delivery of active pharmaceutical ingredients (APIs) over an extended period. These tablets are designed to optimize therapeutic efficacy and improve patient…

Solid Dosage form, Tablets

Ensuring Consistency in Tablet Thickness Across Batches

March 11, 2025 Admin

Ensuring Consistency in Tablet Thickness Across Batches Ensuring Consistency in Tablet Thickness Across Batches Introduction: In the realm of pharmaceutical manufacturing, ensuring the consistency of tablet thickness across batches is paramount to maintaining product quality and patient safety. Tablet thickness is not just a matter of aesthetics; it directly correlates with the tablet’s weight, hardness,…

Solid Dosage form, Tablets

Managing Failures in Residual Solvent Control for Purified Water Systems

March 11, 2025 Admin

Managing Failures in Residual Solvent Control for Purified Water Systems Managing Failures in Residual Solvent Control for Purified Water Systems Introduction: The pharmaceutical industry heavily relies on purified water systems to ensure the quality and efficacy of its products. As such, managing residual solvents in these systems is critical for maintaining product safety and compliance…

Solid Dosage form, Tablets

Troubleshooting Residual Powder Issues in Tablet Compression Equipment During Validation

March 10, 2025 Admin

Troubleshooting Residual Powder Issues in Tablet Compression Equipment During Validation Troubleshooting Residual Powder Issues in Tablet Compression Equipment During Validation Introduction: The pharmaceutical industry is continuously evolving, with tablet manufacturing playing a crucial role in the delivery of medications. One of the significant challenges faced during the tablet compression process is the issue of residual…

Solid Dosage form, Tablets

Addressing Heat Sensitivity of APIs During Validation of Coated Tablets

March 10, 2025 Admin

Addressing Heat Sensitivity of APIs During Validation of Coated Tablets Addressing Heat Sensitivity of APIs During Validation of Coated Tablets Introduction: The pharmaceutical industry continuously strives to enhance the efficacy, stability, and safety of drug products. One of the critical aspects of drug formulation is the management of active pharmaceutical ingredients (APIs) that exhibit sensitivity…

Solid Dosage form, Tablets

Ensuring Consistency in Spray Gun Calibration for Film-Coated Tablet Production

March 9, 2025 Admin

Ensuring Consistency in Spray Gun Calibration for Film-Coated Tablet Production Ensuring Consistency in Spray Gun Calibration for Film-Coated Tablet Production Introduction: The pharmaceutical industry places a high value on precision and consistency, particularly in the production of film-coated tablets. A critical element of this process is the calibration of spray guns used to apply the…

Solid Dosage form, Tablets

Managing Residual Solvent Contamination in Utility Lines for Coated Tablets

March 8, 2025 Admin

Managing Residual Solvent Contamination in Utility Lines for Coated Tablets Managing Residual Solvent Contamination in Utility Lines for Coated Tablets Introduction: Residual solvent contamination in utility lines presents a significant challenge in the production of coated tablets. These solvents, often used in pharmaceutical manufacturing processes, must be carefully managed to ensure product safety, efficacy, and…

Solid Dosage form, Tablets