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Tag: Pharmaceutical Industry

Validating Equipment for High-Speed Compression of Multi-Layer Tablets

Posted on April 6, 2025 By Admin

Validating Equipment for High-Speed Compression of Multi-Layer Tablets Validating Equipment for High-Speed Compression of Multi-Layer Tablets Introduction: In the pharmaceutical industry, the demand for multi-layer tablets has been increasing due to their ability to deliver multiple drugs with different release profiles in a single dosage form. This has led to the need for high-speed compression…

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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

Difficulty in ensuring compliance with capsule stability testing guidelines.

Posted on April 5, 2025 By Admin

Difficulty in ensuring compliance with capsule stability testing guidelines. Difficulty in ensuring compliance with capsule stability testing guidelines. Introduction: In the pharmaceutical industry, ensuring the stability of solid oral dosage forms, particularly capsules, is crucial for maintaining the efficacy, safety, and quality of medications throughout their shelf life. Capsule stability testing serves as a fundamental…

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

Challenges in ensuring proper environmental monitoring during production.

Posted on April 5, 2025 By Admin

Challenges in ensuring proper environmental monitoring during production. Challenges in ensuring proper environmental monitoring during production. Introduction: In the pharmaceutical industry, ensuring the quality and safety of products is of utmost importance. One critical aspect of this is maintaining an optimal production environment to prevent contamination and ensure product efficacy. Environmental monitoring is a systematic…

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

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

Problems with maintaining consistent capsule hardness.

Posted on April 4, 2025 By Admin

Problems with maintaining consistent capsule hardness. Problems with Maintaining Consistent Capsule Hardness Introduction: Capsules, whether hard or soft gelatin, are among the most prevalent forms of solid oral dosage forms in the pharmaceutical industry. Ensuring consistent capsule hardness is crucial as it affects the product’s stability, dissolution rate, and bioavailability. Variability in capsule hardness can…

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

Troubleshooting Root Cause Analysis for Non-Adherence in Stability Studies

Posted on April 3, 2025 By Admin

Troubleshooting Root Cause Analysis for Non-Adherence in Stability Studies Troubleshooting Root Cause Analysis for Non-Adherence in Stability Studies Introduction: Stability studies are a crucial component of the pharmaceutical development process, ensuring that drug products maintain their intended quality, safety, and efficacy throughout their shelf life. Non-adherence to stability protocols can lead to significant issues, including…

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Solid Dosage form, Tablets

Lack of real-time monitoring systems for capsule sealing uniformity.

Posted on April 3, 2025 By Admin

Lack of real-time monitoring systems for capsule sealing uniformity. Lack of real-time monitoring systems for capsule sealing uniformity. Introduction: In the pharmaceutical industry, ensuring the quality and integrity of solid oral dosage forms, particularly capsules, is paramount. Capsules, both hard and soft gelatin types, are a preferred delivery system for many medications due to their…

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

Difficulty in validating capsule drying processes for thermosensitive APIs.

Posted on April 1, 2025 By Admin

Difficulty in validating capsule drying processes for thermosensitive APIs. Difficulty in validating capsule drying processes for thermosensitive APIs Introduction: In the realm of pharmaceutical manufacturing, ensuring the stability and efficacy of Active Pharmaceutical Ingredients (APIs) is paramount. Thermosensitive APIs, which are prone to degradation at elevated temperatures, pose unique challenges. As capsules, especially hard and…

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

Identifying Problems in Potency Testing for Extended Release Tablets

Posted on March 31, 2025 By Admin

Identifying Problems in Potency Testing for Extended Release Tablets Identifying Problems in Potency Testing for Extended Release Tablets Introduction: Extended release tablets are a cornerstone of modern pharmaceutical therapy, providing patients with the convenience of reduced dosing frequency while maintaining therapeutic efficacy over an extended period. Potency testing of these formulations is critical to ensure…

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Solid Dosage form, Tablets

Addressing Die Wear Issues in Tablet Press Machines

Posted on March 30, 2025 By Admin

Addressing Die Wear Issues in Tablet Press Machines Addressing Die Wear Issues in Tablet Press Machines Introduction: In the pharmaceutical industry, the production of tablets is a critical process that demands precision and consistency. Tablet press machines, essential to this process, must operate efficiently to ensure that the tablets produced meet stringent quality standards. One…

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Solid Dosage form, Tablets

Identifying Root Causes of Content Non-Uniformity in Tablets

Posted on March 29, 2025 By Admin

Identifying Root Causes of Content Non-Uniformity in Tablets Identifying Root Causes of Content Non-Uniformity in Tablets Introduction: Content uniformity in tablets is a critical quality attribute that ensures each tablet contains an equal amount of the active pharmaceutical ingredient (API). This consistency is vital for efficacy, safety, and regulatory compliance. The challenge of maintaining content…

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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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