by maheshbhuva | Mar 16, 2023 | ALCOA++, Analytical Chemistry, QMS
GMP Data Integrity ALCOA to ALCOA Plus Plus for Data Integrity in Pharma Guidelines, Principles and Practical Examples for Modern Quality Control Laboratories. 15 min read Singapore (HSA / PIC/S) Focus 1. Introduction: Why Data Integrity is Critical In modern... by maheshbhuva | Feb 6, 2023 | Analytical Chemistry, Deviation, Documents error (DIN), Pharmaceutical interview,, QMS
Wet Lab analyst do Error ! Wet lab analyst are forgot a taken out of LOD or sulphated Ash, weight forgotten, etc ! . Some dilution error !. Weight print are not past in work sheet OR analytical work report or protocol etc (whatever terminology used). ! Calibration... by maheshbhuva | Dec 10, 2022 | Analytical Chemistry, Deviation, Documents error (DIN), Out of specification, Pharmaceutical interview,, QMS
DIN (documents incident) IncidentDeviationOOS DIN Documentary error like miss date and sign, entry missed in logbook, Incident Like power failure, peak shape not properly, baseline not properly et OOS Results was not found as per specification Share this: Share on...