Tag: cleaning processes

Poor reproducibility in swab recovery studies during cleaning validation.

April 22, 2025 Admin

Poor reproducibility in swab recovery studies during cleaning validation. Poor reproducibility in swab recovery studies during cleaning validation. Introduction: Cleaning validation is a critical component of Good Manufacturing Practices (GMP) in the pharmaceutical industry. It ensures that any equipment used in the production of drug products is adequately cleaned to prevent contamination of subsequent batches….

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

Inadequate systems for monitoring cleaning agent residues in rinse water.

March 11, 2025 Admin

Inadequate systems for monitoring cleaning agent residues in rinse water. Inadequate Systems for Monitoring Cleaning Agent Residues in Rinse Water Introduction: Ensuring the cleanliness of pharmaceutical manufacturing equipment is critical to maintaining product safety and efficacy. In the production of solid oral dosage forms, such as capsules, the presence of cleaning agent residues in rinse…

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

Difficulty in validating cleaning processes for high-viscosity formulations.

March 2, 2025 Admin

Difficulty in validating cleaning processes for high-viscosity formulations. Difficulty in Validating Cleaning Processes for High-Viscosity Formulations Introduction: In the pharmaceutical industry, maintaining the integrity and quality of solid oral dosage forms, such as capsules, is of paramount importance. Among these, high-viscosity formulations present unique challenges in the cleaning process validation. This blog delves into the…

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