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Tag: pharmaceutical best practices

Managing Fines Generation During Compression of Immediate Release Tablets

Posted on March 17, 2025 By Admin

Managing Fines Generation During Compression of Immediate Release Tablets Managing Fines Generation During Compression of Immediate Release Tablets Introduction: In the pharmaceutical industry, the production of immediate-release tablets is a crucial process that requires meticulous attention to detail. One of the significant challenges faced during the tablet manufacturing process is the generation of fines. Fines…

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Solid Dosage form, Tablets

Preventing Layer Cracking in Multi-Layer Tablets During Storage

Posted on March 17, 2025 By Admin

Preventing Layer Cracking in Multi-Layer Tablets During Storage Preventing Layer Cracking in Multi-Layer Tablets During Storage Introduction: Multi-layer tablets are an increasingly popular pharmaceutical dosage form due to their ability to deliver multiple active ingredients with different release profiles in a single dosage unit. Despite their benefits, these tablets are susceptible to layer cracking during…

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Solid Dosage form, Tablets

Achieving Uniform Blend Distribution in Blending Machines

Posted on March 17, 2025 By Admin

Achieving Uniform Blend Distribution in Blending Machines Achieving Uniform Blend Distribution in Blending Machines Introduction: In the pharmaceutical industry, ensuring the uniform distribution of active pharmaceutical ingredients (APIs) and excipients in solid dosage forms is critical for product efficacy, safety, and quality. Blending is a key process in tablet manufacturing, where achieving uniform blend distribution…

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Solid Dosage form, Tablets

Ensuring Consistency in Rinse Water Sampling for Cleaning Validation

Posted on March 17, 2025 By Admin

Ensuring Consistency in Rinse Water Sampling for Cleaning Validation Ensuring Consistency in Rinse Water Sampling for Cleaning Validation Introduction: In the pharmaceutical industry, maintaining the highest standards of cleanliness is crucial for ensuring product safety and efficacy. Cleaning validation, particularly rinse water sampling, plays a significant role in verifying that manufacturing equipment is free from…

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Solid Dosage form, Tablets

Troubleshooting Uneven Compression Force in Multi-Layer Tablets

Posted on March 16, 2025 By Admin

Troubleshooting Uneven Compression Force in Multi-Layer Tablets Troubleshooting Uneven Compression Force in Multi-Layer Tablets Introduction: In the pharmaceutical industry, multi-layer tablets represent a crucial innovation, offering benefits such as multiple drug release profiles and combinations in a single dose. However, the manufacturing of these tablets comes with its own set of challenges. One significant issue…

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Solid Dosage form, Tablets

Ensuring Consistency in Dissolution Testing for Multi-API Tablets

Posted on March 16, 2025 By Admin

Ensuring Consistency in Dissolution Testing for Multi-API Tablets Ensuring Consistency in Dissolution Testing for Multi-API Tablets Introduction: Dissolution testing is a critical quality control measure in the pharmaceutical industry, particularly for tablets containing multiple active pharmaceutical ingredients (APIs). Ensuring consistency in dissolution testing is vital as it impacts the tablet’s efficacy, safety, and regulatory compliance….

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Solid Dosage form, Tablets

Preventing Adhesion Failures in Multi-Layer Tablet Compression

Posted on March 16, 2025 By Admin

Preventing Adhesion Failures in Multi-Layer Tablet Compression Preventing Adhesion Failures in Multi-Layer Tablet Compression Introduction: In the pharmaceutical industry, the production of multi-layer tablets has become increasingly popular due to their ability to deliver multiple drugs or release profiles simultaneously. However, one of the significant challenges faced during the manufacturing process is adhesion failure between…

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Solid Dosage form, Tablets

Difficulty in maintaining uniform mixing of powder blends.

Posted on March 16, 2025 By Admin

Difficulty in maintaining uniform mixing of powder blends. Difficulty in maintaining uniform mixing of powder blends. Introduction: In the pharmaceutical industry, achieving uniform mixing of powder blends is paramount for the production of effective and safe solid oral dosage forms, such as capsules and tablets. Uniformity in powder blends ensures consistent drug delivery, efficacy, and…

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

Inadequate systems for monitoring capsule fill weight variations during long-term storage.

Posted on March 16, 2025 By Admin

Inadequate systems for monitoring capsule fill weight variations during long-term storage. Inadequate Systems for Monitoring Capsule Fill Weight Variations During Long-Term Storage Introduction: In the pharmaceutical industry, ensuring the quality and consistency of solid oral dosage forms, particularly capsules, is crucial. Capsules, whether hard or soft gelatin, are popular due to their ease of administration…

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

Addressing Non-Conformance in Weight Variation Tests During QA Audits

Posted on March 15, 2025 By Admin

Addressing Non-Conformance in Weight Variation Tests During QA Audits Addressing Non-Conformance in Weight Variation Tests During QA Audits Introduction: In the realm of pharmaceutical manufacturing, ensuring the quality and consistency of solid dosage forms like tablets is paramount. One critical parameter assessed during quality assurance (QA) audits is the weight variation of tablets. Consistent tablet…

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Solid Dosage form, Tablets

Poor reproducibility in microbial stability results for capsules stored in high-humidity environments.

Posted on March 15, 2025 By Admin

Poor reproducibility in microbial stability results for capsules stored in high-humidity environments. Poor Reproducibility in Microbial Stability Results for Capsules Stored in High-Humidity Environments Introduction: Microbial stability is a critical aspect of pharmaceutical product development, particularly for solid oral dosage forms like capsules. Ensuring the reliability and consistency of microbial stability results is essential to…

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

Managing Excessive Binder Use in Wet Granulation Processes

Posted on March 15, 2025 By Admin

Managing Excessive Binder Use in Wet Granulation Processes Managing Excessive Binder Use in Wet Granulation Processes Introduction: In the pharmaceutical industry, wet granulation is a crucial process used to improve the flowability and compressibility of powder blends, ultimately ensuring the production of high-quality tablets. Binders play an essential role in wet granulation, providing the necessary…

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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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