Reference and Working standard SOP – Handling & Preparation
Introduction to Reference and Working standard Reference and Working standard handling and preparation form the backbone of accurate and reliable
Dehumidifier Performance Qualification: Procedure
Introduction to Dehumidifier Performance Qualification Dehumidifier Performance Qualification – A dehumidifier used in pharmaceutical manufacturing can have a direct impact
Microbial Evaluation of Compressed Air and Gases in Pharma
Introduction to Microbial Evaluation of Compressed Air A suitable microbial evaluation of compressed air and gases helps determine whether the
Chiller Qualification (Water-Cooled Screw) : IQ, OQ and PQ Guide
Introduction to Chiller Qualification Chiller Qualification-A chilled water system can be an important utility in a pharmaceutical manufacturing facility. Chilled
Validation Master Plan (VMP) in Pharmaceuticals
Introduction to Validation Master Plan A Validation Master Plan (VMP) is a controlled document that provides an overall framework for
Analyst Validation in QC: Procedure & Acceptance Criteria
Introduction of Analyst Validation Analyst Validation-Reliable laboratory results depend not only on validated analytical methods and qualified instruments, but also