SOP for Electronic Data Management (Laboratory)
Standard Operating Procedure (SOP) for Electronic data backup, restoration, archival, retrieval and scheduled verification of stored data of quality control.
Audit
cGMP
Checklist / Formats
GLP
Quality Control
SOPs
Audit
cGMP
Checklist / Formats
GLP
QA Sop
SOPs
- February 15, 2020
- by admin
SOP For Handling of Laboratory Incident
SOP for handling and reporting of Laboratory Incident (Lab Event ) occurs in the Quality Control like be-Bracketing standard failure,.
cGMP
Production
SOPs
Stores Sops
- February 9, 2020
- by admin
SOP for Issuance of Packing Material
Standard Operating Procedure for Issuance / Dispensing of Packaging Material (Packing Materials) like Corrugated box, Primary Packaging Material (PPM), Secondary.
Audit
Calibration
cGMP
GLP
SOPs
- February 5, 2020
- by admin
SOP for Handling of Out of Calibration (OOC)
Standard Operating Procedure for Handling of Out of Calibration (OOC) for Laboratory Instrument and Equipment. The result which does not.
cGMP
Checklist
Production
Production Sop
QA Sop
SOPs
- January 29, 2020
- by admin
Acceptable Quality Level (AQL) – SOP and Chart
The Acceptable Quality Level (AQL) is a percent defective that is the baseline requirement for the quality of the producer’s.
cGMP
Checklist / Formats
Protocol
QA Sop
QC Sop
Quality Control
SOPs
- January 25, 2020
- by admin
Stability Study SOP as per ICH Guideline
Stability study sop prepared according to ICH guidelines with required stability study sample incubation, sample pullouts and analysis of samples.
cGMP
Micro Sop
Microbiology
SOPs
- January 18, 2020
- by admin
Isolation and Identification of Microorganisms
Standard Operating Procedure (SOP) for Isolation and Identification of Microorganisms (Microbes). Isolation and Identification of Microorganisms 1.0 PURPOSE:.
cGMP
Checklist / Formats
QA Sop
SOPs
- January 16, 2020
- by admin
SOP for Quality Risk Management (Guideline ICH Q9)
Quality Risk Management: An overall and continuing systematic process for the assessment, control, communication and review of risks to the.
cGMP
Checklist / Formats
QA Sop
SOPs
- January 15, 2020
- by admin
Product Recall Procedure and Format
The drug product recall is a process of removal or correction of marketed products for the reasons relating to deficiencies.
cGMP
SOPs
Stores Sops
- January 8, 2020
- by admin
Receipt and Storage of Raw Material
Standard Operating procedure for receipt and storage of raw material. Starting material such as API and excipient required in the.
