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Tag: solid dosage forms

Managing Material Shrinkage in Heat-Sealed Tablet Pouches

Posted on March 16, 2025 By Admin

Managing Material Shrinkage in Heat-Sealed Tablet Pouches Managing Material Shrinkage in Heat-Sealed Tablet Pouches Introduction: In the pharmaceutical industry, the packaging of solid dosage forms such as tablets is crucial for maintaining their integrity, efficacy, and shelf life. Heat-sealed tablet pouches are a popular choice due to their protective properties and ease of use. However,…

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Solid Dosage form, Tablets

Difficulty in maintaining uniform mixing of powder blends.

Posted on March 16, 2025 By Admin

Difficulty in maintaining uniform mixing of powder blends. Difficulty in maintaining uniform mixing of powder blends. Introduction: In the pharmaceutical industry, achieving uniform mixing of powder blends is paramount for the production of effective and safe solid oral dosage forms, such as capsules and tablets. Uniformity in powder blends ensures consistent drug delivery, efficacy, and…

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

Ensuring Even Coating Thickness in Irregularly Shaped Tablets

Posted on March 16, 2025 By Admin

Ensuring Even Coating Thickness in Irregularly Shaped Tablets Ensuring Even Coating Thickness in Irregularly Shaped Tablets Introduction: In the pharmaceutical industry, tablets are a widely used solid dosage form due to their convenience, stability, and ease of mass production. Coating these tablets serves multiple purposes, including masking unpleasant tastes, enhancing swallowability, and protecting the active…

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Solid Dosage form, Tablets

Addressing API Variability Issues During Quality Assurance Audits

Posted on March 16, 2025 By Admin

Addressing API Variability Issues During Quality Assurance Audits Addressing API Variability Issues During Quality Assurance Audits Introduction: In the pharmaceutical industry, ensuring the consistency and reliability of Active Pharmaceutical Ingredients (APIs) is crucial, especially during quality assurance audits. API variability can significantly impact the safety, efficacy, and quality of the final product, making it a…

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Solid Dosage form, Tablets

Addressing Non-Conformance in Weight Variation Tests During QA Audits

Posted on March 15, 2025 By Admin

Addressing Non-Conformance in Weight Variation Tests During QA Audits Addressing Non-Conformance in Weight Variation Tests During QA Audits Introduction: In the realm of pharmaceutical manufacturing, ensuring the quality and consistency of solid dosage forms like tablets is paramount. One critical parameter assessed during quality assurance (QA) audits is the weight variation of tablets. Consistent tablet…

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Solid Dosage form, Tablets

Managing Failures in Weight Uniformity Tests for High-Speed Compression

Posted on March 15, 2025 By Admin

Managing Failures in Weight Uniformity Tests for High-Speed Compression Managing Failures in Weight Uniformity Tests for High-Speed Compression Introduction: The pharmaceutical industry is ever-evolving, with the demand for high-quality and efficient production processes constantly on the rise. High-speed compression in tablet manufacturing is a critical process, crucial for meeting market demands and ensuring patient safety….

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Solid Dosage form, Tablets

Resolving Failures in Moisture Content Tests for Sugar-Coated Tablets

Posted on March 14, 2025 By Admin

Resolving Failures in Moisture Content Tests for Sugar-Coated Tablets Resolving Failures in Moisture Content Tests for Sugar-Coated Tablets Introduction: In the pharmaceutical industry, sugar-coated tablets are a popular dosage form due to their aesthetic appeal and ability to mask unpleasant tastes. However, maintaining the correct moisture content in these tablets is crucial, as it affects…

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Solid Dosage form, Tablets

Troubleshooting Residual Binder Issues in Granulation Equipment During Validation

Posted on March 14, 2025 By Admin

Troubleshooting Residual Binder Issues in Granulation Equipment During Validation Troubleshooting Residual Binder Issues in Granulation Equipment During Validation Introduction: In the pharmaceutical industry, ensuring the quality and efficacy of solid dosage forms like tablets is paramount. Granulation is a critical process in tablet manufacturing, where powders are agglomerated to form granules, enhancing flowability and compressibility…

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Solid Dosage form, Tablets

Troubleshooting Variability in Dissolution Profiles During Stability Studies

Posted on March 14, 2025 By Admin

Troubleshooting Variability in Dissolution Profiles During Stability Studies Troubleshooting Variability in Dissolution Profiles During Stability Studies Introduction: Dissolution testing is a critical aspect of pharmaceutical development, acting as a quality control measure to ensure that tablets release their active ingredients at the intended rate and extent. During stability studies, the variability in dissolution profiles can…

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Solid Dosage form, Tablets

Challenges in validating uniform mixing of multi-component powder blends.

Posted on March 14, 2025 By Admin

Challenges in validating uniform mixing of multi-component powder blends. Challenges in validating uniform mixing of multi-component powder blends. Introduction: In the pharmaceutical industry, ensuring the uniform mixing of multi-component powder blends is crucial for maintaining the quality and efficacy of solid oral dosage forms, such as capsules and tablets. The uniformity of the blend directly…

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

Troubleshooting Loss of Moisture Control in Hygroscopic Tablet Storage

Posted on March 14, 2025 By Admin

Troubleshooting Loss of Moisture Control in Hygroscopic Tablet Storage Troubleshooting Loss of Moisture Control in Hygroscopic Tablet Storage Introduction: In the pharmaceutical industry, maintaining the integrity of solid dosage forms, particularly hygroscopic tablets, is crucial. Hygroscopic tablets are designed to absorb moisture from the environment, making them particularly vulnerable to degradation if not stored properly….

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Solid Dosage form, Tablets

Troubleshooting Non-Adherence of Coating Materials in Enteric Tablets

Posted on March 13, 2025 By Admin

Troubleshooting Non-Adherence of Coating Materials in Enteric Tablets Troubleshooting Non-Adherence of Coating Materials in Enteric Tablets Introduction: Enteric tablets are specially designed solid dosage forms that remain intact in the acidic environment of the stomach and dissolve in the more neutral pH of the intestine. This ensures that active pharmaceutical ingredients (APIs) are released at…

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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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