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Author: Admin

Troubleshooting Thickness Testing Failures in Enteric-Coated Tablets

Posted on March 26, 2025 By Admin

Troubleshooting Thickness Testing Failures in Enteric-Coated Tablets Troubleshooting Thickness Testing Failures in Enteric-Coated Tablets Introduction: Enteric-coated tablets are a critical component in the pharmaceutical industry, designed to deliver active ingredients to the intestines without being degraded by stomach acid. The integrity of this enteric coating is vital, and one key quality parameter is the thickness…

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Solid Dosage form, Tablets

Ensuring Consistency in API Release Profiles for Controlled Release Tablets

Posted on March 26, 2025 By Admin

Ensuring Consistency in API Release Profiles for Controlled Release Tablets Ensuring Consistency in API Release Profiles for Controlled Release Tablets Introduction: In the world of pharmaceuticals, controlled release tablets play a pivotal role in ensuring the therapeutic efficacy of drugs. These formulations are designed to release active pharmaceutical ingredients (APIs) at a predetermined rate, maintaining…

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Solid Dosage form, Tablets

High rejection rates due to non-compliance with quality standards.

Posted on March 26, 2025 By Admin

High rejection rates due to non-compliance with quality standards. High Rejection Rates Due to Non-Compliance with Quality Standards Introduction: In the pharmaceutical industry, maintaining high-quality standards in manufacturing processes is imperative. Solid oral dosage forms, particularly capsules, are prevalent due to their convenience and efficiency. However, the rejection rates of these products can often spike…

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

Managing Solvent Levels in Film-Coating Processes for Consistency

Posted on March 26, 2025 By Admin

Managing Solvent Levels in Film-Coating Processes for Consistency Managing Solvent Levels in Film-Coating Processes for Consistency Introduction: In the pharmaceutical industry, the film-coating process of tablets is a crucial step that ensures not only the aesthetic appeal but also the stability and controlled release of the active pharmaceutical ingredients (APIs). Managing solvent levels during this…

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Solid Dosage form, Tablets

How to Optimize Spray Rate for Uniform Tablet Coating

Posted on March 26, 2025 By Admin

How to Optimize Spray Rate for Uniform Tablet Coating How to Optimize Spray Rate for Uniform Tablet Coating Why is Spray Rate Important in Tablet Coating? The spray rate is a critical parameter in the tablet coating process, determining the uniformity, consistency, and quality of the coating layer. An optimized spray rate ensures that the…

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Tablets

Optimization of Anti-Adherent Agents in Film Coating

Posted on March 26, 2025 By Admin

Optimization of Anti-Adherent Agents in Film Coating Step-by-Step Guide to Optimizing Anti-Adherent Agents in Film Coating Overview: Film coating is an essential step in tablet manufacturing, improving drug stability, taste masking, and controlled drug release. However, one of the most common issues faced during coating is tablet sticking and adhesion, leading to poor-quality coatings, inconsistent…

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Tablets

Managing Residual Solvents in Solvent-Based Coating Applications

Posted on March 26, 2025 By Admin

Managing Residual Solvents in Solvent-Based Coating Applications Managing Residual Solvents in Solvent-Based Coating Applications Introduction: The use of solvent-based coatings in the pharmaceutical industry plays a crucial role in enhancing the stability, appearance, and functionality of solid dosage forms such as tablets. However, managing residual solvents in these applications is paramount to ensure the safety,…

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Solid Dosage form, Tablets

Challenges in validating cleaning processes for aqueous-based capsule formulations.

Posted on March 26, 2025 By Admin

Challenges in validating cleaning processes for aqueous-based capsule formulations. Challenges in validating cleaning processes for aqueous-based capsule formulations Introduction: In the pharmaceutical industry, ensuring the cleanliness of manufacturing equipment is paramount, especially when dealing with aqueous-based capsule formulations. These formulations, found in both hard and soft gelatin capsules, pose unique challenges due to their propensity…

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

Solubility Testing of Drug Candidates

Posted on March 26, 2025 By Admin

Solubility Testing of Drug Candidates Guide to Solubility Testing of Drug Candidates Ensuring Effective Drug Delivery Through Solubility Assessment Solubility is a key factor in the bioavailability of drug candidates, influencing their absorption, distribution, and overall effectiveness. Solubility testing is essential in preclinical studies to evaluate how well a drug dissolves in a specific solvent,…

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Drug Discovery

Managing Powder Segregation in High-Speed Blending Equipment

Posted on March 25, 2025 By Admin

Managing Powder Segregation in High-Speed Blending Equipment Managing Powder Segregation in High-Speed Blending Equipment Introduction: In the pharmaceutical industry, achieving uniformity in solid dosage forms is crucial for ensuring efficacy and patient safety. High-speed blending equipment is commonly used in the production of tablets to mix powdered ingredients. However, one of the significant challenges in…

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Solid Dosage form, Tablets

Poor validation of water purification systems for high-demand operations.

Posted on March 25, 2025 By Admin

Poor validation of water purification systems for high-demand operations. Poor validation of water purification systems for high-demand operations. Introduction: Water purification systems are integral to pharmaceutical manufacturing, especially in the production of solid oral dosage forms like capsules. The quality of water used directly impacts the safety and efficacy of oral medications. However, poor validation…

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

Managing Particle Size Reduction in High-Dose API Tablet Formulations

Posted on March 25, 2025 By Admin

Managing Particle Size Reduction in High-Dose API Tablet Formulations Expert Guide to Managing Particle Size Reduction in High-Dose API Tablet Formulations Why is Particle Size Reduction Important in High-Dose API Formulations? Particle size reduction is a critical step in the formulation of high-dose active pharmaceutical ingredient (API) tablets. Reducing the particle size of the API…

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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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