Industrial Hygiene – SOP & Guideline
The Standard Operating Procedure (SOP) to describe the various aspect of Industrial Hygiene in pharmaceutical drug manufacturing plants. Industrial Hygiene
Audit
Environment
Health & Safety (EHS)
SOPs
Audit
cGMP
Checklist
GLP
Maintenance Sops
QA Sop
SOPs
Validation
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
GLP
QC Sop
Quality Control
SOPs
Entry and Exit Procedure in QC Laboratory
Standard Operating Procedure (SOP) for Entry and Exit Procedure in Quality Control (QC) Laboratory in a pharmaceutical plant. Entry and
Maintenance Sops
SOPs
Operation Procedure of 1010 KVA DG Set
Standard Operating Procedure (SOP) for the operation of 1010 KVA Diesel Generating – DG Set installed for power backup in
cGMP
QA Sop
SOPs
Stores Sops
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
GLP
Micro Sop
Microbiology
SOPs
Purified Water – Sampling and Testing Procedure
Standard Operating Procedure (SOP) for sampling from different points and microbiological analysis/testing of Purified water samples in pharmaceutical plants. Sampling
cGMP
Checklist / Formats
GLP
Micro Sop
Microbiology
QC Sop
Quality Control
SOPs
Analyst Qualification SOP in Quality Control
Standard Operating Procedure (SOP) for Analyst/Chemist Qualification, Data Reviewer Qualification through performing parallel Analysis, and other evaluation parameters. Download SOP
Calibration
GLP
HPLC
QC Sop
Quality Control
SOPs
Waters HPLC System-Operation SOP with Empower
Standard Operating System (SOP) for Operation of Waters High-Performance Liquid Chromatography (HPLC) system. This procedure applies to the Waters –
cGMP
Checklist / Formats
Production
QA Sop
SOPs
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
Production Sop
SOPs
Inspection and Handling of Sieves and Screens
Standard Operating Practices (SOP) for the receipt, checking, passivation, storage, and disposal (handling) of Sieves/Screens. Procedure for Handling of Sieves
