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Tag: Regulatory compliance

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

Validating Clean Steam Systems for Sustained Release Tablet Coating Machines

Posted on June 3, 2025 By Admin

Validating Clean Steam Systems for Sustained Release Tablet Coating Machines Validating Clean Steam Systems for Sustained Release Tablet Coating Machines Introduction: In the pharmaceutical industry, the precision and reliability of equipment are crucial to ensuring product efficacy and safety. Among these, sustained release tablet coating machines play a pivotal role in controlling the release profile…

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Solid Dosage form, Tablets

Managing Packing Material Variation for Consistency in Blister Packaging

Posted on June 3, 2025 By Admin

Managing Packing Material Variation for Consistency in Blister Packaging Managing Packing Material Variation for Consistency in Blister Packaging Introduction: In the pharmaceutical industry, blister packaging serves as a critical component for ensuring the stability and protection of solid dosage forms like tablets. The packaging not only safeguards the medication but also ensures patient compliance and…

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Solid Dosage form, Tablets

Validating Cleanroom HVAC Systems for Enteric-Coated Tablet Manufacturing

Posted on June 2, 2025 By Admin

Validating Cleanroom HVAC Systems for Enteric-Coated Tablet Manufacturing Validating Cleanroom HVAC Systems for Enteric-Coated Tablet Manufacturing Introduction: In the pharmaceutical industry, the manufacturing of enteric-coated tablets requires stringent environmental controls to ensure product integrity and patient safety. The role of Heating, Ventilation, and Air Conditioning (HVAC) systems in maintaining cleanroom conditions is critical. These systems…

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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

Managing Residue Build-Up in Spray Guns for Coating Equipment Cleaning Validation

Posted on May 31, 2025 By Admin

Managing Residue Build-Up in Spray Guns for Coating Equipment Cleaning Validation Managing Residue Build-Up in Spray Guns for Coating Equipment Cleaning Validation Introduction: In the pharmaceutical industry, maintaining the integrity of coating equipment is vital for ensuring product quality and regulatory compliance. Spray guns, integral to the coating process, often face challenges related to residue…

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Solid Dosage form, Tablets

Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets

Posted on May 31, 2025 By Admin

Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets Introduction: Dissolution testing is a critical quality control measure in the pharmaceutical industry, especially for coated tablets. It ensures that the drug releases its active ingredients at the intended rate and extent. However, calibration failures…

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Solid Dosage form, Tablets

Investigating Impact of Humidity on Coating Integrity in Film-Coated Tablets

Posted on May 31, 2025 By Admin

Investigating Impact of Humidity on Coating Integrity in Film-Coated Tablets Investigating Impact of Humidity on Coating Integrity in Film-Coated Tablets Introduction: In the pharmaceutical industry, ensuring the integrity of film-coated tablets is a critical aspect of product quality and efficacy. Film coatings on tablets serve multiple purposes, including protection from environmental factors, masking unpleasant tastes,…

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Solid Dosage form, Tablets

Validating Water Purification Systems for Tablet Manufacturing Processes

Posted on May 30, 2025 By Admin

Validating Water Purification Systems for Tablet Manufacturing Processes Validating Water Purification Systems for Tablet Manufacturing Processes Introduction: In the pharmaceutical industry, water is not just an ingredient; it is a critical component in the manufacturing of tablets. The purity and quality of water used in tablet manufacturing are paramount, as they directly affect the safety…

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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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