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Tag: pharmaceutical quality

Validating Adequacy of Binder Distribution in Compression Processes

Posted on March 9, 2025 By Admin

Validating Adequacy of Binder Distribution in Compression Processes Validating Adequacy of Binder Distribution in Compression Processes Introduction: In the pharmaceutical industry, ensuring the quality and efficacy of solid dosage forms such as tablets is paramount. A critical aspect of this is the distribution of binders during the compression process. Binders play a key role in…

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Solid Dosage form, Tablets

Real-Time Adjustment of Granulation Parameters for Uniformity

Posted on March 9, 2025 By Admin

Real-Time Adjustment of Granulation Parameters for Uniformity Real-Time Adjustment of Granulation Parameters for Uniformity Introduction: In the pharmaceutical industry, the uniformity of granulation is critical for ensuring the quality and efficacy of solid dosage forms, particularly tablets. Granulation is a pivotal step in the tablet manufacturing process, where powder particles are aggregated to form granules….

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Solid Dosage form, Tablets

Addressing Coating Peel-Off During Stability Studies

Posted on March 8, 2025 By Admin

Addressing Coating Peel-Off During Stability Studies Addressing Coating Peel-Off During Stability Studies Introduction: In the realm of pharmaceutical manufacturing, ensuring the stability and integrity of tablet coatings is paramount. Coatings play a crucial role in protecting the active pharmaceutical ingredient (API), controlling release profiles, improving patient compliance, and enhancing the aesthetic appeal of the product….

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Solid Dosage form, Tablets

Validating Adequacy of Binder Concentration in Wet Granulation Processes

Posted on March 8, 2025 By Admin

Validating Adequacy of Binder Concentration in Wet Granulation Processes Validating Adequacy of Binder Concentration in Wet Granulation Processes Introduction: In the realm of pharmaceutical manufacturing, the wet granulation process is a cornerstone for producing high-quality tablets. Ensuring the adequacy of binder concentration is critical in this process, as it directly influences the tablet’s integrity, dissolution…

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Solid Dosage form, Tablets

Preventing Non-Uniform API Distribution in Multi-API Tablets

Posted on March 8, 2025 By Admin

Preventing Non-Uniform API Distribution in Multi-API Tablets Preventing Non-Uniform API Distribution in Multi-API Tablets Introduction: In the intricate world of pharmaceutical manufacturing, ensuring the uniform distribution of Active Pharmaceutical Ingredients (APIs) within multi-API tablets is crucial. These tablets are essential for delivering multiple therapeutic effects simultaneously, often improving patient compliance. However, achieving uniform API distribution…

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Solid Dosage form, Tablets

Detecting Core Erosion in Sugar-Coated Tablets During Coating Processes

Posted on March 8, 2025 By Admin

Detecting Core Erosion in Sugar-Coated Tablets During Coating Processes Detecting Core Erosion in Sugar-Coated Tablets During Coating Processes Introduction: The pharmaceutical industry relies heavily on the integrity and efficacy of solid dosage forms like tablets. Among these, sugar-coated tablets have been traditionally used for their aesthetic appeal and ability to mask unpleasant tastes. However, the…

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Solid Dosage form, Tablets

Troubleshooting Failures in Humidity Control for Compression Equipment Areas

Posted on March 8, 2025 By Admin

Troubleshooting Failures in Humidity Control for Compression Equipment Areas Troubleshooting Failures in Humidity Control for Compression Equipment Areas Introduction: In the pharmaceutical industry, maintaining precise environmental control in manufacturing areas is crucial, especially in compression equipment zones used for tablet production. Humidity control is a significant aspect of this environment, as fluctuations can lead to…

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Solid Dosage form, Tablets

Addressing Layer Delamination Issues During Disintegration Testing

Posted on March 8, 2025 By Admin

Addressing Layer Delamination Issues During Disintegration Testing Addressing Layer Delamination Issues During Disintegration Testing Introduction: In the world of pharmaceuticals, ensuring the integrity of solid dosage forms like tablets is of utmost importance. Layer delamination, a challenge often encountered during disintegration testing, can compromise the efficacy and safety of a pharmaceutical product. This phenomenon occurs…

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Solid Dosage form, Tablets

Difficulty in validating capsule filling for lipid-based formulations.

Posted on March 8, 2025 By Admin

Difficulty in validating capsule filling for lipid-based formulations. Difficulty in Validating Capsule Filling for Lipid-Based Formulations Introduction: Lipid-based formulations have gained significant attention in the pharmaceutical industry due to their potential to improve the bioavailability of poorly soluble drugs. As a result, encapsulating these formulations, particularly in hard or soft gelatin capsules, has become increasingly…

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

Controlling Binder Distribution in Wet Granulation Processes

Posted on March 7, 2025 By Admin

Controlling Binder Distribution in Wet Granulation Processes Controlling Binder Distribution in Wet Granulation Processes Introduction: In the pharmaceutical industry, the wet granulation process is a critical method for producing tablets. It involves the agglomeration of powder particles using a liquid binder, which helps improve the flow and compaction properties of the powder mix. However, the…

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Solid Dosage form, Tablets

Troubleshooting Non-Uniform Disintegration in Coated Tablets During Testing

Posted on March 7, 2025 By Admin

Troubleshooting Non-Uniform Disintegration in Coated Tablets During Testing Troubleshooting Non-Uniform Disintegration in Coated Tablets During Testing Introduction: Coated tablets are a prevalent form of medication delivery in the pharmaceutical industry, designed to improve the stability, appearance, and release characteristics of the active pharmaceutical ingredient (API). The disintegration of these tablets is a critical quality attribute…

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Solid Dosage form, Tablets

Managing Static Charge in Powder Handling Systems During Production

Posted on March 7, 2025 By Admin

Managing Static Charge in Powder Handling Systems During Production Managing Static Charge in Powder Handling Systems During Production Introduction: In the world of pharmaceutical manufacturing, maintaining the integrity and safety of production processes is paramount. One often overlooked but critical aspect is the management of static charge in powder handling systems. Static electricity can cause…

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Solid Dosage form, Tablets

Posts pagination

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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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