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Tag: Pharmaceutical manufacturing

Validating Agglomeration Control Measures in Fluid Bed Granulation Processes

Posted on March 2, 2025 By 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…

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Solid Dosage form, Tablets

Addressing Coating Delamination Issues During In-Process Quality Checks

Posted on March 2, 2025 By Admin

Addressing Coating Delamination Issues During In-Process Quality Checks Addressing Coating Delamination Issues During In-Process Quality Checks Introduction: In the pharmaceutical industry, tablets are one of the most common solid dosage forms. The coating of these tablets plays a pivotal role not only in aesthetics but also in functionality, including protection from environmental conditions, masking taste,…

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Solid Dosage form, Tablets

Managing Cleaning Validation Failures for Immediate Release Tablet Equipment

Posted on March 2, 2025 By Admin

Managing Cleaning Validation Failures for Immediate Release Tablet Equipment Managing Cleaning Validation Failures for Immediate Release Tablet Equipment Introduction: In the pharmaceutical industry, ensuring the cleanliness of manufacturing equipment is critical to product quality and safety. Particularly for immediate release tablets, stringent cleaning protocols prevent cross-contamination and guarantee that residue levels remain within acceptable limits….

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Solid Dosage form, Tablets

Addressing Residual Solvent Issues in Compressed Air Lines for Enteric Tablets

Posted on March 2, 2025 By Admin

Addressing Residual Solvent Issues in Compressed Air Lines for Enteric Tablets Addressing Residual Solvent Issues in Compressed Air Lines for Enteric Tablets Introduction: In the pharmaceutical industry, maintaining the purity and quality of solid dosage forms, particularly enteric tablets, is crucial. Enteric tablets, designed to withstand the acidic environment of the stomach and dissolve in…

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Solid Dosage form, Tablets

Managing Punch Adhesion Issues in Tablet Pressing Operations

Posted on March 2, 2025 By Admin

Managing Punch Adhesion Issues in Tablet Pressing Operations Managing Punch Adhesion Issues in Tablet Pressing Operations Introduction: The process of tablet pressing is a critical stage in the production of solid dosage forms. One of the common issues faced during this process is punch adhesion, which can significantly affect the quality and consistency of the…

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Solid Dosage form, Tablets

Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring

Posted on March 2, 2025 By Admin

Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring Introduction: In the pharmaceutical industry, maintaining a pristine environment is paramount to ensuring product quality and patient safety. Cleanrooms play a crucial role in this process, particularly in the manufacturing of solid dosage forms like tablets. A…

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Solid Dosage form, Tablets

Resolving Weight Variation Failures in Bilayer Tablets

Posted on March 2, 2025 By 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….

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Solid Dosage form, Tablets

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

Posted on March 2, 2025 By 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…

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Solid Dosage form, Tablets

Addressing Color Fading in Sugar-Coated Tablets During Accelerated Testing

Posted on March 2, 2025 By Admin

Addressing Color Fading in Sugar-Coated Tablets During Accelerated Testing Addressing Color Fading in Sugar-Coated Tablets During Accelerated Testing Introduction: In the pharmaceutical industry, the aesthetic and functional integrity of sugar-coated tablets is paramount. The coating not only enhances the appearance but also affects consumer perception and compliance. However, during accelerated stability testing, a crucial phase…

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Solid Dosage form, Tablets

Validating Steam Sterilization Systems for Coating Pans in Multi-Product Facilities

Posted on March 2, 2025 By Admin

Validating Steam Sterilization Systems for Coating Pans in Multi-Product Facilities Validating Steam Sterilization Systems for Coating Pans in Multi-Product Facilities Introduction: In the complex world of pharmaceutical manufacturing, ensuring the sterility of equipment is crucial for product safety and efficacy. This is particularly true in multi-product facilities, where cross-contamination risks are heightened. One critical piece…

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Solid Dosage form, Tablets

Poor reproducibility in capsule placement within tray compartments.

Posted on March 2, 2025 By Admin

Poor reproducibility in capsule placement within tray compartments. Poor reproducibility in capsule placement within tray compartments. Introduction: In the pharmaceutical industry, the precision of solid oral dosage forms is crucial for ensuring product quality and patient safety. Capsules, whether hard or soft gelatin, are a popular choice due to their convenience and ability to encapsulate…

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

Managing Over-Lubrication in Blending Processes for Compression

Posted on March 2, 2025 By 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…

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Solid Dosage form, Tablets

Posts pagination

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  • Aerosol Formulations
  • Capsules (Hard & Soft Gelatin)
  • Drug Discovery
  • External Preparations
  • GLP Guidelines
  • GMP Guidelines
  • Medical Devices
  • Parenteral Drug Manufacturing
  • Pharma Quality Control
  • Pharma Research
  • Schedule M
  • Solid Dosage form
  • Solid Oral Dosage Forms
  • Tablets
  • Tablets

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