RISK ASSESSMENT FOR QC INSTRUMENTS

A Risk Assessment for QC instruments in the pharmaceutical industry is critical to ensure accurate, reliable, and compliant data. The purpose of this assessment is to identify, assess, and mitigate potential risks associated with the use, maintenance, and performance of QC Instruments used for Pharmaceutical testing. The scope of this assessment covers all analytical instruments used in the QC laboratory.

GENERAL LABORATORY INSTRUMENTS

1. Risk Assessment for Analytical Weighing Balance
2. Risk Assessment for pH Meter
3. Risk Assessment for Conductivity Meter
4. Risk Assessment for TOC Analyser
5. Risk Assessment for Refrigerator
6. Risk Assessment for Water Purification System

ANALYTICAL INSTRUMENTS

1. Risk Assessment for Gas Chromatography
2. Risk Assessment for HPLC
3. Risk Assessment for UV – Vis Spectrophotometer
4. Risk Assessment for FTIR
5. Risk Assessment for Karl Fischer

PHYSICAL TESTING INSTRUMENTS

1. Risk Assessment for Dissolution Test Apparatus
2. Risk Assessment for Disintegration Test Apparatus
3. Risk Assessment for Friability Test Apparatus
4. Risk Assessment for Hardness Tester
5. Risk Assessment for Bulk Density Apparatus
6. Risk Assessment for Melting Point Apparatus
7. Risk Assessment for Hot Air Oven
8. Risk Assessment for Moisture Analyser
9. Risk Assessment for Viscometer