Author: pharmajia

VENDOR AUDIT 0

Vendor Audit: A Comprehensive Approach to Risk Management

This article describes for Vendor Audits/vendor qualification for Active Pharmaceutical ingredients (APIs), Excipients, Packing Material and evaluation of approved manufacturers of API’s, Excipients & Packing Material. Detailed procedure for Vendor Audits / Vendor Qualification....

Different Dosage forms 0

Sop for Analysis of different Dosage forms

This Document describes (Standard Operating procedure) Sop for Analysis of different Dosage forms of manufactured products. Sop for Analysis of different Dosage forms of manufactured products. I. Purpose & Scope: The Purpose of this...

Quality control procedures 0

Sop for Quality control procedures

This Document describes (Standard Operating procedure) Sop for Quality control procedures. Sop for Quality control procedures. I. PURPOSE AND SCOPE: The Purpose of this SOP is to lay down the procedure to lay down working...

Calibration of FTIR 0

Sop for Operation and Calibration of FTIR

This Document describes (Standard Operating procedure) Sop for Operation and Calibration of FTIR Sop for Operation and Calibration of FTIR I. Purpose & Scope: The Purpose of this SOP is to lay down the...

Vacuum pump for filtration 0

Sop for Vacuum pump for filtration

This Document describes (Standard Operating procedure) Sop for Operation and Calibration of Vacuum Pump for filtration. Sop for Operation and Calibration of Vacuum Pump for filtration I. Purpose & Scope: The Purpose of this...