Ensuring Quality Control in Pharmaceutical Processes

Quality control (QC) can be a significant challenge for pharmaceutical laboratories. Without a robust system for ensuring product quality, labs will have a higher margin for error, be prone to falling out of compliance with regulations, and are subject to losing time in regulatory inspections.

This series will share insight that QC lab leaders can implement as part of their QC processes, including how to minimize human errors, effectively responding to questions from regulators, and how a new HPLC system can mitigate common errors in liquid chromatography.