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Tag: Pharmaceutical Industry

Addressing Non-Compliance in Process Validation for Hygroscopic Tablets

Posted on June 4, 2025 By Admin

Addressing Non-Compliance in Process Validation for Hygroscopic Tablets Addressing Non-Compliance in Process Validation for Hygroscopic Tablets Introduction: In the pharmaceutical industry, the process validation of hygroscopic tablets presents unique challenges. Hygroscopic tablets are those that have a tendency to absorb moisture from their surroundings, which can lead to significant issues in their stability, efficacy, and…

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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

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 Spray Gun Settings for Even Coating Distribution

Posted on June 1, 2025 By Admin

Validating Spray Gun Settings for Even Coating Distribution Validating Spray Gun Settings for Even Coating Distribution Introduction: In the pharmaceutical industry, ensuring that tablets have an even coating is crucial not only for aesthetic purposes but also for the functionality of the dosage form. The coating protects the active pharmaceutical ingredient (API), controls release profiles,…

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Solid Dosage form, Tablets

Troubleshooting Folding Defects in Patient Information Leaflets

Posted on May 31, 2025 By Admin

Troubleshooting Folding Defects in Patient Information Leaflets Troubleshooting Folding Defects in Patient Information Leaflets Introduction: Patient Information Leaflets (PILs) are critical components in pharmaceutical packaging, providing essential information about the medication’s usage, dosage, and potential side effects. However, folding defects in these leaflets can lead to serious implications, including miscommunication of drug information, non-compliance with…

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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

Ensuring Alignment of Tablets in Blister Packs for Aesthetic Appeal

Posted on May 29, 2025 By Admin

Ensuring Alignment of Tablets in Blister Packs for Aesthetic Appeal Ensuring Alignment of Tablets in Blister Packs for Aesthetic Appeal Introduction: In the competitive pharmaceutical market, aesthetics and functionality of packaging play a crucial role in consumer perception and product success. Ensuring the proper alignment of tablets within blister packs not only enhances visual appeal…

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Solid Dosage form, Tablets

Managing Failures in Process Validation for High-Speed Compression

Posted on May 27, 2025 By Admin

Managing Failures in Process Validation for High-Speed Compression Managing Failures in Process Validation for High-Speed Compression Introduction: In the pharmaceutical industry, process validation is a critical component of quality assurance, particularly for high-speed compression in tablet manufacturing. This process ensures that tablets meet consistent standards for quality, safety, and efficacy. However, managing failures in process…

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Solid Dosage form, Tablets

Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation

Posted on May 27, 2025 By Admin

Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation Introduction: In the realm of pharmaceutical manufacturing, bilayer tablets have emerged as a significant advancement, offering multiple benefits such as the ability to combine incompatible substances, controlled release profiles, and patient convenience. However, the manufacturing…

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Solid Dosage form, Tablets

Validating Batch Records for Regulatory Compliance in Tablet Manufacturing

Posted on May 25, 2025 By Admin

Validating Batch Records for Regulatory Compliance in Tablet Manufacturing Validating Batch Records for Regulatory Compliance in Tablet Manufacturing Introduction: In the pharmaceutical industry, ensuring the integrity and accuracy of batch records is paramount, particularly in the manufacturing of tablets. Batch records serve as a critical component in the documentation of each step of the manufacturing…

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Solid Dosage form, Tablets

Ensuring Robustness in Disintegration Time During Validation Testing

Posted on May 24, 2025 By Admin

Ensuring Robustness in Disintegration Time During Validation Testing Ensuring Robustness in Disintegration Time During Validation Testing Introduction: In the pharmaceutical industry, the disintegration time of tablets is a critical quality attribute that directly impacts drug release and bioavailability. Ensuring robustness in disintegration time during validation testing is essential to maintain consistency in therapeutic efficacy and…

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Solid Dosage form, Tablets

Ensuring Consistency in Packaging Material Thickness for Stability

Posted on May 23, 2025 By Admin

Ensuring Consistency in Packaging Material Thickness for Stability Ensuring Consistency in Packaging Material Thickness for Stability Introduction: In the pharmaceutical industry, maintaining the stability of solid dosage forms like tablets is crucial. Packaging plays a vital role in ensuring product stability by protecting the contents from environmental factors such as moisture, oxygen, and light. Consistency…

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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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