Tag: Quality Systems

Troubleshooting Friability Failures During Technical Transfer: Insights on Tooling, Granulation, and Lubrication In the realm of pharmaceutical manufacturing, friability failures during technical transfer can pose significant challenges. When tablet formulations…

Addressing Friability Failures during CPV Review: Troubleshooting Tooling, Granulation, and Lubrication Issues Friability failure during a Continuous Process Verification (CPV) review can significantly impact batch quality and regulatory compliance in…

Steps for Investigating Disintegration Failure Post Scale-Up in Pharmaceutical Manufacturing Disintegration failures following scale-up present critical challenges for pharmaceutical manufacturers. Such failures often lead to out-of-specification (OOS) test results, delays…

Understanding Tablet Lamination Challenges Post Scale-Up: A Guide for Compliance and Investigation In the pharmaceutical manufacturing space, tablet lamination can emerge as a significant issue following the scale-up phase. This…

Addressing Disintegration Failures for FDA Inspection Readiness: Effective Sampling Plans to Prevent OOS Disintegration testing is a critical quality control measure for oral solid dosage forms, such as tablets and…

Addressing Friability Failures Observed After Stability Pulls: An In-Depth Investigation In pharmaceutical manufacturing, the stability of solid oral dosage forms, such as tablets and capsules, is critical for ensuring product…

Analyzing Capsule Fill Weight Variation Following Stability Testing: Ensuring Compliance with Regulatory Expectations The pharmaceutical industry frequently encounters challenges during regulatory compliance, especially concerning stability studies that impact capsule fill…

Addressing Tablet Capping Issues Following Scale-Up: A Comprehensive Investigation Framework Tablet capping is a significant manufacturing concern that can arise during the scale-up of solid oral dosage forms. This article…

Addressing Weight Variation Issues Following Equipment Maintenance in Pharmaceutical Manufacturing In the highly regulated environment of pharmaceutical manufacturing, maintaining product quality is paramount. Weight variation issues, particularly after maintenance activities,…

Understanding and Documenting Hardness Drift Following Excipient Changes in Pharmaceutical Manufacturing In the realm of pharmaceutical manufacturing, the quality attributes of solid oral dosage forms, such as tablets and capsules,…

Challenges in Tablet Lamination Following Scale-Up: Investigating Process Parameter Limits and Validation Effects Quality assurance teams in pharmaceutical manufacturing often face challenges during the scale-up of tablet lamination processes. An…

Investigating Disintegration Failures during Continuous Process Verification Reviews In pharmaceutical manufacturing, ensuring the integrity and efficacy of solid oral dosage forms, such as tablets and capsules, is crucial. A common…