Handling of Rejected Raw and Packing Materials
Standard Operating Procedure (SOP) for the handling of rejected raw materials and packing materials which are rejected due to the.
cGMP
QA Sop
Quality Control
SOPs
Stores Sops
cGMP
Checklist
Checklist / Formats
Production
Production Sop
QA Sop
- September 17, 2020
- by admin
Reconciliation of Packing Materials and Bulk-SOP
Standard Operating Procedure (SOP) for reconciliation of packing materials and bulk at the end of the packing of each batch.
cGMP
Health & Safety (EHS)
Maintenance Sops
Micro Sop
QA Sop
QC Sop
SOPs
Validation
- September 16, 2020
- by admin
Purified Water Plant – Operation and Regeneration
Standard Operating Procedure (SOP) to define the procedure for operation and regeneration of the Purified Water Plant (Mixed bed unit)..
cGMP
GLP
Health & Safety (EHS)
Production
Production Sop
QA Sop
QC Sop
Quality Control
SOPs
- September 14, 2020
- by admin
Residual Solvent Limit in Raw Material (API) – SOP
Residual solvent in pharmaceuticals is defined here as organic volatile chemicals that are used or produced in the manufacture of.
cGMP
Checklist / Formats
Protocol
QA Sop
SOPs
Validation
- September 13, 2020
- by admin
SOP for Protocol and Report Numbering System
Standard Operating System (SOP) issuance, controlling, and management of different Protocols and its numbering System in pharmaceuticals for different activities..
cGMP
Checklist / Formats
GLP
QA Sop
SOPs
- September 12, 2020
- by admin
Specimen Signature Recording SOP of Employee
Standard Operating Procedure (SOP) for the recording of Specimen Signatures of Employees and contract personnel. Specimen Signature is a copy.
cGMP
Checklist
Checklist / Formats
Environment
Health & Safety (EHS)
Production
Production Sop
QA Sop
QC Sop
SOPs
Validation
- September 9, 2020
- by admin
New Product Introduction (Risk Evaluation)
This SOP provides guidance to evaluate the potential of the proposed new product for cross-contamination and assessment of the containment.
Audit
cGMP
Checklist
Checklist / Formats
Doc
Environment
Health & Safety (EHS)
Maintenance Sops
Micro Sop
Microbiology
Production
Production Sop
QA Sop
QC Sop
Quality Control
SOPs
Sterile
Validation
- August 31, 2020
- by admin
Cross Contamination, Mix-Ups & Microbial Contamination
Standard Operating Procedure (SOP) and Detailed Risk Assessment approach for Prevention of Cross Contamination, Mix-ups, and Microbial Contamination. Download SOP.
Audit
cGMP
Doc
GLP
Maintenance Sops
Micro Sop
Microbiology
Production
Production Sop
Protocol
QA Sop
QC Sop
Quality Control
Research
SOPs
Uncategorized
- August 27, 2020
- by admin
Good Documentation Practices – SOP & Guideline
Standard Operating Procedure (SOP) cum Guideline for Good Documentation Practices for cGxP documents (Electronic and Handwritten) Pharmaceutical Drug Manufacturing Plants..
Calibration
cGMP
GLP
Production
Production Sop
QA Sop
SOPs
Validation
- August 19, 2020
- by admin
Calibration Program – SOP & Policy
Standard Operating Procedure (SOP) and Policy/Program for Calibration of Instrument, Equipment, and Measuring Device used to measurement, monitoring, and controlling.
