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Tag: pharmaceutical quality assurance]

Ensuring Robustness in Disintegration Tests for High-Dose Tablets

Posted on March 5, 2025 By Admin

Ensuring Robustness in Disintegration Tests for High-Dose Tablets Ensuring Robustness in Disintegration Tests for High-Dose Tablets Introduction: In the pharmaceutical industry, high-dose tablets serve as a critical vehicle for delivering therapeutic agents effectively. Disintegration tests are essential for ensuring that these tablets dissolve appropriately, releasing their active ingredients for absorption. For high-dose tablets, achieving reliable…

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Solid Dosage form, Tablets

Addressing Non-Compliance in Utility Validation for Hygroscopic Tablet Production

Posted on March 5, 2025 By Admin

Addressing Non-Compliance in Utility Validation for Hygroscopic Tablet Production Addressing Non-Compliance in Utility Validation for Hygroscopic Tablet Production Introduction: In the pharmaceutical industry, producing high-quality tablets that meet regulatory standards is crucial. Among various tablet forms, hygroscopic tablets present unique challenges due to their moisture sensitivity. Utility validation is a vital part of ensuring that…

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Solid Dosage form, Tablets

Validating Water for Injection Systems for Enteric-Coated Tablet Equipment

Posted on March 4, 2025 By Admin

Validating Water for Injection Systems for Enteric-Coated Tablet Equipment Validating Water for Injection Systems for Enteric-Coated Tablet Equipment Introduction: In the pharmaceutical industry, the production of enteric-coated tablets demands a high level of precision and adherence to quality standards. One crucial aspect of this process is the validation of Water for Injection (WFI) systems, which…

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Solid Dosage form, Tablets

Addressing High Friability in Sugar-Coated Tablets

Posted on March 4, 2025 By Admin

Addressing High Friability in Sugar-Coated Tablets Addressing High Friability in Sugar-Coated Tablets Introduction: Sugar-coated tablets are a popular solid dosage form due to their appealing appearance, taste masking capabilities, and ability to protect the drug core from environmental factors. However, achieving the ideal balance between coating thickness and tablet robustness is crucial to maintain product…

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Solid Dosage form, Tablets

Ensuring Adequacy of Cleanroom Pressure Differentials During Validation

Posted on March 4, 2025 By Admin

Ensuring Adequacy of Cleanroom Pressure Differentials During Validation Ensuring Adequacy of Cleanroom Pressure Differentials During Validation Introduction: In the pharmaceutical industry, maintaining a contamination-free environment is crucial for ensuring the safety and efficacy of products. Cleanrooms, with their controlled environments, are critical in achieving this objective. One of the key aspects of cleanroom management is…

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Solid Dosage form, Tablets

Validating Steam Quality for Fluid Bed Granulators in Multi-Product Facilities

Posted on March 4, 2025 By Admin

Validating Steam Quality for Fluid Bed Granulators in Multi-Product Facilities Validating Steam Quality for Fluid Bed Granulators in Multi-Product Facilities Introduction: In the complex landscape of pharmaceutical manufacturing, ensuring the highest quality of products is paramount. One critical aspect of this process is the validation of steam quality, particularly in multi-product facilities where fluid bed…

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Solid Dosage form, Tablets

Inadequate validation protocols for new capsule formulations.

Posted on March 4, 2025 By Admin

Inadequate validation protocols for new capsule formulations. Inadequate Validation Protocols for New Capsule Formulations Introduction: The pharmaceutical industry is continually evolving, with innovations leading to new and effective drug delivery systems. Among these, capsules remain a popular choice due to their ease of administration and ability to encapsulate a wide range of drug compounds. However,…

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

Ensuring Robustness in Cleaning Validation for Granulators Used with Low-Dose APIs

Posted on March 4, 2025 By Admin

Ensuring Robustness in Cleaning Validation for Granulators Used with Low-Dose APIs Ensuring Robustness in Cleaning Validation for Granulators Used with Low-Dose APIs Introduction: In the pharmaceutical industry, ensuring the cleanliness and safety of manufacturing equipment is crucial, especially when dealing with low-dose Active Pharmaceutical Ingredients (APIs). Granulators, essential in the tablet production process, must undergo…

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Solid Dosage form, Tablets

Challenges in implementing robust quality controls for capsule packaging processes.

Posted on March 4, 2025 By Admin

Challenges in implementing robust quality controls for capsule packaging processes. Challenges in implementing robust quality controls for capsule packaging processes. Introduction: The pharmaceutical industry prioritizes patient safety and product efficacy, making quality control a critical component of the manufacturing process. Capsules, both hard and soft gelatin, are among the most common solid oral dosage forms….

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

Problems with detecting improper sealing in high-viscosity formulations.

Posted on March 4, 2025 By Admin

Problems with detecting improper sealing in high-viscosity formulations. Problems with Detecting Improper Sealing in High-Viscosity Formulations Introduction: In pharmaceutical manufacturing, ensuring the integrity of solid oral dosage forms is paramount. Capsules, both hard and soft gelatin, are popular due to their versatility and patient compliance. However, when dealing with high-viscosity formulations, improper sealing poses significant…

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

Ensuring Compliance with Regulatory Standards for Clean Steam Quality

Posted on March 3, 2025 By Admin

Ensuring Compliance with Regulatory Standards for Clean Steam Quality Ensuring Compliance with Regulatory Standards for Clean Steam Quality Introduction: In the pharmaceutical industry, clean steam is a critical component used in various processes, including sterilization and humidification. Ensuring compliance with regulatory standards for clean steam quality is essential to maintain the safety and efficacy of…

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Solid Dosage form, Tablets

Troubleshooting Non-Uniform Coating in Irregular Tablet Shapes

Posted on March 3, 2025 By Admin

Troubleshooting Non-Uniform Coating in Irregular Tablet Shapes Troubleshooting Non-Uniform Coating in Irregular Tablet Shapes Introduction: In the intricate world of pharmaceutical manufacturing, ensuring the uniformity of tablet coatings is paramount, particularly when dealing with irregular tablet shapes. These coatings are not just for aesthetic appeal; they serve critical functions such as protecting the tablet’s core,…

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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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