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Tag: Equipment Design

Difficulty in establishing validated cleaning procedures for semi-solid formulations.

Posted on April 30, 2025 By Admin

Difficulty in establishing validated cleaning procedures for semi-solid formulations. Difficulty in Establishing Validated Cleaning Procedures for Semi-Solid Formulations Introduction: In the pharmaceutical industry, maintaining cleanliness and avoiding cross-contamination are paramount, particularly when dealing with semi-solid formulations. These formulations, which include creams, ointments, gels, and pastes, present unique challenges in terms of cleaning validation due to…

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

Troubleshooting Failures in Cleaning Validation for Multi-Layer Tablet Equipment

Posted on April 12, 2025 By Admin

Troubleshooting Failures in Cleaning Validation for Multi-Layer Tablet Equipment Troubleshooting Failures in Cleaning Validation for Multi-Layer Tablet Equipment Introduction: In the pharmaceutical industry, maintaining the cleanliness of equipment is crucial for ensuring product safety and efficacy. Cleaning validation is a critical aspect of Good Manufacturing Practices (GMP) that ensures that equipment used in the production…

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Solid Dosage form, Tablets

Problems with validating cleaning procedures for encapsulation equipment.

Posted on April 2, 2025 By Admin

Problems with validating cleaning procedures for encapsulation equipment. Problems with validating cleaning procedures for encapsulation equipment. Introduction: In the pharmaceutical industry, maintaining the cleanliness of manufacturing equipment is critical to ensuring product quality and patient safety. Encapsulation equipment, used extensively for producing both hard and soft gelatin capsules, poses unique challenges when it comes to…

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

Managing Powder Segregation in High-Speed Blending Equipment

Posted on March 25, 2025 By Admin

Managing Powder Segregation in High-Speed Blending Equipment Managing Powder Segregation in High-Speed Blending Equipment Introduction: In the pharmaceutical industry, achieving uniformity in solid dosage forms is crucial for ensuring efficacy and patient safety. High-speed blending equipment is commonly used in the production of tablets to mix powdered ingredients. However, one of the significant challenges in…

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Solid Dosage form, Tablets

Troubleshooting Static Charge in Powder Handling Systems

Posted on March 16, 2025 By Admin

Troubleshooting Static Charge in Powder Handling Systems Troubleshooting Static Charge in Powder Handling Systems Introduction: In the pharmaceutical industry, the handling of powders is a critical step in the production of solid dosage forms, particularly tablets. However, a common and often challenging issue that arises during this process is the buildup of static charge. Static…

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Solid Dosage form, Tablets

Managing Fines Generation in Fluid Bed Processing

Posted on March 9, 2025 By Admin

Managing Fines Generation in Fluid Bed Processing Managing Fines Generation in Fluid Bed Processing Introduction: Fluid bed processing is a critical operation in pharmaceutical manufacturing, primarily utilized for drying, granulating, and coating purposes. Its efficiency and effectiveness in producing uniform and quality granules make it a preferred choice in tablet production. However, a persistent challenge…

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Solid Dosage form, Tablets

Managing Cleaning Validation for Spray Coating Machines with Complex Designs

Posted on March 8, 2025 By Admin

Managing Cleaning Validation for Spray Coating Machines with Complex Designs Managing Cleaning Validation for Spray Coating Machines with Complex Designs Introduction: In the pharmaceutical industry, maintaining the highest standards of cleanliness and hygiene is imperative to ensure product safety and efficacy. Cleaning validation is a critical aspect of pharmaceutical manufacturing, particularly for spray coating machines…

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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
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