Batch Processing – SOP & General Check Points
.perating Procedure (SOP) for General Check Point during Drug Product Batch Processing in the pharmaceuticals drug manufacturing plant. General Checks.
cGMP
Checklist
Checklist / Formats
Production
Production Sop
QA Sop
SOPs
Calibration
cGMP
Checklist / Formats
GLP
QA Sop
QC Sop
Quality Control
SOPs
- June 13, 2020
- by admin
Stability Chamber – Operation, Cleaning and Performance check
Standard Operating procedure (SOP) for Operation, Cleaning, and Performance Check/Calibration of Stability chamber (Oven) used for the stability study of.
Audit
cGMP
Checklist
GLP
Maintenance Sops
QA Sop
SOPs
Validation
- June 1, 2020
- by admin
Physical & Logical Control Policy of Computer System
Standard Operating Procedure (SOP) for Physical and Logical Control Policy of Computer system to fulfill the requirement of 21CFR Part.
cGMP
QA Sop
SOPs
Stores Sops
- May 25, 2020
- by admin
Raw Material Reconciliation SOP
Standard Operating Procedure (SOP) for Raw Material Reconciliation in the warehouse/store department in pharmaceuticals to maintain the stock of raw.
cGMP
Checklist / Formats
Production
QA Sop
SOPs
- May 16, 2020
- by admin
Master Batch Record (MBR) – SOP
Standard Operating Procedure (SOP) for preparation, review, approval, issuance, maintenance, and archival of controlled Master Batch Record (MBR) throughout the.
cGMP
Production Sop
QA Sop
SOPs
Validation
- April 29, 2020
- by admin
Handling of Hold Time Drug Samples
Standard Operating Procedure (SOP) to establish the hold time of drug samples at the different stages of manufacturing (like starting.
cGMP
Checklist / Formats
Production
Production Sop
Protocol
QA Sop
Research
SOPs
- April 8, 2020
- by admin
SOP for Handling of Market Complaint
Standard Operating Procedure (SOP) for Handling of Market Complaint of Finished Pharmaceutical Drug Product. A market/consumer complaint is a notification.
cGMP
Checklist
Checklist / Formats
Production
Production Sop
QA Sop
SOPs
- March 28, 2020
- by admin
SOP for Line Clearance (LC) of Area and Equipments
Standard Operating Procedure (SOP) for Line Clearance (LC) of the manufacturing area and equipment at the different stages of drug.
