Tag: pharma QA

Addressing Viscosity Drift in Accelerated Stability Testing: A Systematic Investigation Viscosity drift observed during accelerated stability testing is a critical concern in the pharmaceutical industry, especially for dental dosage forms.…

Investigating pH Drift Post-Packaging Change: Strategies for Ensuring Compatibility and Stability In the pharmaceutical manufacturing environment, a pH drift following a packaging change can present significant challenges, particularly regarding product…

Analyzing Phase Separation Occurrences During Method Transfer: A Comprehensive Guide for Quality Assurance Review Phase separation in pharmaceutical manufacturing can significantly impact quality, particularly during method transfer processes. This article…

Investigation into Texture Grittiness Complaints Following a Packaging Change In pharmaceutical manufacturing, quality complaints such as texture grittiness can indicate underlying issues that can impact product quality and patient satisfaction.…

Investigation of Tube Leakage Complaints during Method Transfer: Ensuring Packaging Compatibility and Justifying Shelf Life In the realm of pharmaceutical manufacturing, particularly within the domain of dosage forms, tube leakage…

E&L Failures Post-Supplier Change: Implementing Robust Sampling and Mixing Controls When a supplier is changed in pharmaceutical manufacturing, it can lead to significant risks, including extractables and leachables (E&L) failures.…

Addressing Microbial Limits Failures During Method Transfer: A Comprehensive Investigation Guide Challenges in microbial limit testing are frequent topics of concern in pharmaceutical manufacturing, particularly during method transfer processes. When…

Managing Texture Grittiness Complaints: A Comprehensive Guide for Pharmaceutical Investigations Pharmaceutical professionals are often confronted with complaints regarding product quality, particularly texture grittiness in dosage forms after a change in…