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Tag: pharmaceutical quality assurance]

Managing Residual Moisture Issues in Dryers During Cleaning Validation Studies

Posted on June 5, 2025 By Admin

Managing Residual Moisture Issues in Dryers During Cleaning Validation Studies Managing Residual Moisture Issues in Dryers During Cleaning Validation Studies Introduction: In the pharmaceutical industry, ensuring the cleanliness and safety of manufacturing equipment is crucial to maintaining product integrity and patient safety. Residual moisture in dryers, used in the production of solid dosage forms like…

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Solid Dosage form, Tablets

Investigating Moisture Absorption Issues in Hygroscopic Tablets During Storage

Posted on June 5, 2025 By Admin

Investigating Moisture Absorption Issues in Hygroscopic Tablets During Storage Investigating Moisture Absorption Issues in Hygroscopic Tablets During Storage Introduction: In the vast realm of pharmaceuticals, hygroscopic tablets represent a unique challenge due to their propensity to absorb moisture from the environment. This absorption can lead to significant stability issues, affecting the efficacy and safety of…

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Solid Dosage form, Tablets

Ensuring Accuracy in Rinse Sampling for Coating Machine Validation

Posted on June 3, 2025 By Admin

Ensuring Accuracy in Rinse Sampling for Coating Machine Validation Ensuring Accuracy in Rinse Sampling for Coating Machine Validation Introduction: In the pharmaceutical industry, ensuring the cleanliness and proper validation of coating machines is crucial for both product quality and regulatory compliance. Rinse sampling is a critical component of the cleaning validation process, particularly for coating…

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Solid Dosage form, Tablets

Addressing Residual Solvent Issues in Compressed Air Lines for Enteric Tablets

Posted on June 3, 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

Addressing Challenges in Handling Enteric-Coated Tablets During Blister Packing

Posted on June 2, 2025 By Admin

Addressing Challenges in Handling Enteric-Coated Tablets During Blister Packing Addressing Challenges in Handling Enteric-Coated Tablets During Blister Packing Introduction: Enteric-coated tablets are designed to withstand the acidic environment of the stomach and dissolve in the alkaline environment of the intestine. This specialized coating is crucial for the targeted delivery of certain medications, ensuring their efficacy…

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Solid Dosage form, Tablets

Troubleshooting Failures in Compressed Air Quality Tests for Compression Machines

Posted on June 2, 2025 By Admin

Troubleshooting Failures in Compressed Air Quality Tests for Compression Machines Troubleshooting Failures in Compressed Air Quality Tests for Compression Machines Introduction: In the pharmaceutical industry, the quality of compressed air used in tablet compression machines is paramount. Compressed air serves as a critical utility, influencing both product quality and operational efficiency. Ensuring that this air…

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Solid Dosage form, Tablets

Troubleshooting Failures in Cleaning Validation for Coating Equipment

Posted on June 1, 2025 By Admin

Troubleshooting Failures in Cleaning Validation for Coating Equipment Troubleshooting Failures in Cleaning Validation for Coating Equipment Introduction: In the pharmaceutical industry, the cleaning validation of coating equipment is a critical process that ensures the safety and efficacy of drug products. Cleaning validation verifies that residues from the manufacturing process, including active pharmaceutical ingredients (APIs), excipients,…

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Solid Dosage form, Tablets

Troubleshooting Over-Lubrication in Powder Blends During Compression Validation

Posted on June 1, 2025 By Admin

Troubleshooting Over-Lubrication in Powder Blends During Compression Validation Troubleshooting Over-Lubrication in Powder Blends During Compression Validation Introduction: In the pharmaceutical industry, the production of tablets is a complex process that demands precision and careful attention to detail. One critical aspect of tablet manufacturing is the lubrication of powder blends, which facilitates the tablet compression process….

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Solid Dosage form, Tablets

Validating Cleaning Protocols for High-Speed Compression Lines

Posted on May 28, 2025 By Admin

Validating Cleaning Protocols for High-Speed Compression Lines Validating Cleaning Protocols for High-Speed Compression Lines Introduction: In the pharmaceutical industry, ensuring the cleanliness of equipment used in tablet production is crucial for maintaining product quality and safety. High-speed compression lines are integral to the efficient production of tablets, but they also pose significant challenges when it…

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Solid Dosage form, Tablets

Addressing Failures in Weight Variation Control During Compression Equipment Validation

Posted on May 26, 2025 By Admin

Addressing Failures in Weight Variation Control During Compression Equipment Validation Addressing Failures in Weight Variation Control During Compression Equipment Validation Introduction: In the pharmaceutical industry, ensuring the consistency and quality of products is paramount, especially when it comes to solid dosage forms such as tablets. One critical aspect of tablet manufacturing is weight variation control…

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Solid Dosage form, Tablets

Addressing Brittleness in Sugar-Coated Tablets During Validation Studies

Posted on May 25, 2025 By Admin

Addressing Brittleness in Sugar-Coated Tablets During Validation Studies Addressing Brittleness in Sugar-Coated Tablets During Validation Studies Introduction: Sugar-coated tablets have long been a popular choice in pharmaceutical manufacturing due to their aesthetic appeal, ease of swallowing, and ability to mask the taste of active ingredients. However, the process of sugar coating can introduce brittleness, posing…

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Solid Dosage form, Tablets

Troubleshooting Powder Segregation Issues During Validation of Compression Lines

Posted on May 25, 2025 By Admin

Troubleshooting Powder Segregation Issues During Validation of Compression Lines Troubleshooting Powder Segregation Issues During Validation of Compression Lines Introduction: In the realm of pharmaceutical manufacturing, maintaining the uniformity and consistency of solid dosage forms, such as tablets, is crucial. One of the common challenges faced during the validation of compression lines is powder segregation. This…

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Solid Dosage form, Tablets

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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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