Tag: pharmaceutical industry guidelines

Lack of validated protocols for testing highly hydrophobic APIs.

April 2, 2025 Admin

Lack of validated protocols for testing highly hydrophobic APIs. Lack of validated protocols for testing highly hydrophobic APIs. Introduction: In the pharmaceutical industry, the development and testing of Active Pharmaceutical Ingredients (APIs) are crucial for ensuring drug efficacy and safety. However, one significant challenge that researchers and formulators face is dealing with highly hydrophobic APIs,…

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

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

March 15, 2025 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…

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

Managing Failures in Weight Uniformity Tests for High-Speed Compression

March 15, 2025 Admin

Managing Failures in Weight Uniformity Tests for High-Speed Compression Managing Failures in Weight Uniformity Tests for High-Speed Compression Introduction: The pharmaceutical industry is ever-evolving, with the demand for high-quality and efficient production processes constantly on the rise. High-speed compression in tablet manufacturing is a critical process, crucial for meeting market demands and ensuring patient safety….

Solid Dosage form, Tablets