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Tag: solid dosage forms

Ensuring Adequacy of Binder Distribution in Sustained Release Tablet Validation

Posted on April 19, 2025 By Admin

Ensuring Adequacy of Binder Distribution in Sustained Release Tablet Validation Ensuring Adequacy of Binder Distribution in Sustained Release Tablet Validation Introduction: In the complex world of pharmaceutical manufacturing, sustained release tablets represent a crucial advancement in medication delivery systems. These tablets offer numerous benefits, including improved patient compliance and enhanced bioavailability. However, the validation of…

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Solid Dosage form, Tablets

Ensuring API Stability in Freeze-Thaw Cycles for Temperature-Sensitive Tablets

Posted on April 19, 2025 By Admin

Ensuring API Stability in Freeze-Thaw Cycles for Temperature-Sensitive Tablets Ensuring API Stability in Freeze-Thaw Cycles for Temperature-Sensitive Tablets Introduction: Active Pharmaceutical Ingredients (APIs) are the heart of any medication, providing the therapeutic effect intended for the patient. In the realm of solid dosage forms, particularly tablets, preserving the stability of APIs is crucial. Temperature-sensitive tablets,…

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Solid Dosage form, Tablets

Ensuring Robustness in Compression Force Settings During Validation Processes

Posted on April 18, 2025 By Admin

Ensuring Robustness in Compression Force Settings During Validation Processes Ensuring Robustness in Compression Force Settings During Validation Processes Introduction: In the pharmaceutical industry, ensuring the robustness of compression force settings during the validation of tablet production is crucial. Compression force is a critical parameter that affects the mechanical strength, dissolution, and overall quality of the…

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Solid Dosage form, Tablets

Addressing Root Cause Analysis for Failures in Weight Variation Tests

Posted on April 17, 2025 By Admin

Addressing Root Cause Analysis for Failures in Weight Variation Tests Addressing Root Cause Analysis for Failures in Weight Variation Tests Introduction: In the pharmaceutical industry, ensuring the consistency and quality of solid dosage forms like tablets is paramount. One critical quality control measure is the weight variation test, which evaluates the uniformity of tablet weights…

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Solid Dosage form, Tablets

Challenges in ensuring consistent capsule coating thickness during validation.

Posted on April 16, 2025 By Admin

Challenges in ensuring consistent capsule coating thickness during validation. Challenges in ensuring consistent capsule coating thickness during validation. Introduction: In the pharmaceutical industry, capsules are a prevalent solid oral dosage form due to their ease of administration and ability to deliver precise dosages. Both hard and soft gelatin capsules can be coated for various reasons…

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

Validating Equipment Calibration for Tablet Compression Machines

Posted on April 15, 2025 By Admin

Validating Equipment Calibration for Tablet Compression Machines Validating Equipment Calibration for Tablet Compression Machines Introduction: In the pharmaceutical industry, the production of tablets is a critical process that relies heavily on the precision and accuracy of tablet compression machines. These machines must be meticulously calibrated to ensure that each tablet produced meets the stringent standards…

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Solid Dosage form, Tablets

Problems with ensuring consistent performance of dehumidification systems.

Posted on April 12, 2025 By Admin

Problems with ensuring consistent performance of dehumidification systems. Problems with ensuring consistent performance of dehumidification systems. Introduction: In the manufacturing of solid oral dosage forms, particularly capsules, maintaining the right environmental conditions is crucial. Dehumidification systems play a significant role in ensuring that humidity levels are optimal for processes such as mixing, encapsulation, and storage….

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

Inadequate systems for detecting powder segregation during mixing.

Posted on April 10, 2025 By Admin

Inadequate systems for detecting powder segregation during mixing. Inadequate Systems for Detecting Powder Segregation During Mixing Introduction: In the pharmaceutical industry, ensuring the homogeneity of powder mixtures is crucial for the consistency and efficacy of solid oral dosage forms, particularly capsules. Powder segregation during mixing can lead to significant quality control issues, impacting the uniformity…

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

Addressing Core Erosion in Sugar-Coated Tablets During Validation Runs

Posted on April 8, 2025 By Admin

Addressing Core Erosion in Sugar-Coated Tablets During Validation Runs Addressing Core Erosion in Sugar-Coated Tablets During Validation Runs Introduction: Sugar-coated tablets have been a staple in the pharmaceutical industry, offering a palatable and aesthetically pleasing way to deliver medications. However, the process of sugar coating can present unique challenges, particularly during validation runs, a critical…

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Solid Dosage form, Tablets

Resolving Non-Homogeneity in API Distribution in Multi-API Tablets

Posted on April 6, 2025 By Admin

Resolving Non-Homogeneity in API Distribution in Multi-API Tablets Resolving Non-Homogeneity in API Distribution in Multi-API Tablets Introduction: In the dynamic sphere of pharmaceutical manufacturing, ensuring the consistent distribution of Active Pharmaceutical Ingredients (APIs) within multi-API tablets is crucial. These tablets, designed to deliver multiple therapeutic effects, require precise formulation to ensure that each dose is…

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Solid Dosage form, Tablets

Resolving Moisture Absorption Issues in Hygroscopic Tablets During Storage

Posted on April 4, 2025 By Admin

Resolving Moisture Absorption Issues in Hygroscopic Tablets During Storage Resolving Moisture Absorption Issues in Hygroscopic Tablets During Storage Introduction: In the pharmaceutical industry, hygroscopic tablets present unique challenges due to their propensity to absorb moisture from the environment. This characteristic can adversely affect the stability, efficacy, and shelf life of the medication. Understanding and mitigating…

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Solid Dosage form, Tablets

Difficulty in validating cleaning cycles for gelatin drying trays.

Posted on April 3, 2025 By Admin

Difficulty in validating cleaning cycles for gelatin drying trays. Difficulty in Validating Cleaning Cycles for Gelatin Drying Trays Introduction: In the pharmaceutical industry, ensuring the cleanliness of equipment is paramount to maintaining product integrity and patient safety. Gelatin drying trays, used extensively in the production of hard and soft gelatin capsules, present unique challenges in…

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

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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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