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Tag: pharmaceutical stability

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

Managing API Degradation in Sugar-Coated Tablets During Stability Studies

Posted on June 4, 2025 By Admin

Managing API Degradation in Sugar-Coated Tablets During Stability Studies Managing API Degradation in Sugar-Coated Tablets During Stability Studies Introduction: In the pharmaceutical industry, ensuring the stability and efficacy of a drug product throughout its shelf life is of paramount importance. Sugar-coated tablets, a popular dosage form due to their aesthetic appeal and ease of ingestion,…

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Solid Dosage form, Tablets

Addressing Cracking in Film Coatings of Extended Release Tablets Under Stress

Posted on May 30, 2025 By Admin

Addressing Cracking in Film Coatings of Extended Release Tablets Under Stress Addressing Cracking in Film Coatings of Extended Release Tablets Under Stress Introduction: Film coatings are a critical component in the development of extended-release tablets, playing an essential role in the control of drug release rates, protection of the drug from environmental factors, and improving…

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Solid Dosage form, Tablets

Evaluating Effect of Packaging Interactions on Stability of Sustained Release Tablets

Posted on May 30, 2025 By Admin

Evaluating Effect of Packaging Interactions on Stability of Sustained Release Tablets Evaluating Effect of Packaging Interactions on Stability of Sustained Release Tablets Introduction: In the pharmaceutical industry, ensuring the stability of sustained release tablets is paramount to maintaining efficacy and safety. These tablets are designed to release active ingredients over an extended period, offering advantages…

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Solid Dosage form, Tablets

Ensuring Consistent Release Profiles in Multi-API Tablets Over Time

Posted on May 27, 2025 By Admin

Ensuring Consistent Release Profiles in Multi-API Tablets Over Time Ensuring Consistent Release Profiles in Multi-API Tablets Over Time Introduction: In the pharmaceutical industry, the formulation and manufacturing of multi-API (Active Pharmaceutical Ingredient) tablets present a complex challenge. Ensuring consistent drug release profiles over time is crucial for therapeutic efficacy and patient safety. A consistent release…

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Solid Dosage form, Tablets

Resolving Brittleness in Immediate Release Tablets During Long-Term Storage

Posted on May 26, 2025 By Admin

Resolving Brittleness in Immediate Release Tablets During Long-Term Storage Resolving Brittleness in Immediate Release Tablets During Long-Term Storage Introduction: Immediate release tablets are a cornerstone of pharmaceutical dosage forms, designed to disintegrate promptly after administration to ensure rapid drug release. However, maintaining their integrity during long-term storage poses significant challenges. One of the most critical…

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Solid Dosage form, Tablets

Troubleshooting Non-Conformance in Dissolution Testing Protocols

Posted on May 26, 2025 By Admin

Troubleshooting Non-Conformance in Dissolution Testing Protocols Troubleshooting Non-Conformance in Dissolution Testing Protocols Introduction: Dissolution testing plays a crucial role in the pharmaceutical industry, ensuring that solid dosage forms like tablets release their active ingredients at the desired rate. When these protocols encounter non-conformance, it can lead to significant setbacks in drug development and manufacturing. Understanding…

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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

Evaluating Interaction Between Packaging and Tablets in Stability Testing

Posted on May 21, 2025 By Admin

Evaluating Interaction Between Packaging and Tablets in Stability Testing Evaluating Interaction Between Packaging and Tablets in Stability Testing Introduction: In the pharmaceutical industry, the stability of a drug product is a critical factor that determines its safety, efficacy, and shelf life. Solid dosage forms, like tablets, are particularly sensitive to environmental factors such as humidity,…

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Solid Dosage form, Tablets

Investigating Solvent Evaporation Effects on Coated Tablets During Storage

Posted on May 13, 2025 By Admin

Investigating Solvent Evaporation Effects on Coated Tablets During Storage Investigating Solvent Evaporation Effects on Coated Tablets During Storage Introduction: In the pharmaceutical industry, the stability and integrity of coated tablets during storage are paramount to ensuring their efficacy and safety. Solvent evaporation is a critical factor that can affect the coating’s performance, leading to potential…

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Solid Dosage form, Tablets

Investigating API Potency Retention in Immediate Release Tablets Over Time

Posted on May 11, 2025 By Admin

Investigating API Potency Retention in Immediate Release Tablets Over Time Investigating API Potency Retention in Immediate Release Tablets Over Time Introduction: In the pharmaceutical industry, ensuring the efficacy and safety of medicinal products is paramount. One critical aspect of this is the potency retention of the Active Pharmaceutical Ingredient (API) in immediate release tablets over…

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Solid Dosage form, Tablets

Managing API Migration in Multi-API Tablets During Stability Testing

Posted on May 11, 2025 By Admin

Managing API Migration in Multi-API Tablets During Stability Testing Managing API Migration in Multi-API Tablets During Stability Testing Introduction: In the ever-evolving world of pharmaceuticals, the development of multi-active pharmaceutical ingredient (API) tablets has gained significant momentum. These formulations offer the advantage of delivering multiple therapeutic effects in a single dose, enhancing patient compliance and…

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Solid Dosage form, Tablets

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  • 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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