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,.
Audit
Checklist
Checklist / Formats
Quality Control
SOPs
- February 12, 2020
- by admin
SOP for Review of Analytical Report and Raw Data
Standard Operating Procedure (SOP) for Review of Analytical Report and Raw Data. Analytical raw data is data generated during sample.
Calibration
Checklist / Formats
GLP
Micro Sop
Microbiology
QC Sop
Quality Control
SOPs
- February 8, 2020
- by admin
Operation and Calibration of pH Meter
Standard Operating Procedure (SOP) for Operation, standardization, calibration, and maintenance of pH meter including pH meter electrode care. SOP for.
Checklist
Checklist / Formats
Micro Sop
Microbiology
SOPs
Sterile
- January 30, 2020
- by admin
Checklist for Review of Microbiology Data
Checklist for review of microbiology data generated during the different tests of microbiology i.e. Antibiotic Assays, Particulate matter test, BET.
Audit
Checklist
Checklist / Formats
Doc
GC
GLP
HPLC
- January 28, 2020
- by admin
Checklist for Review of Analytical Raw Data (Chemical)
Checklist for review of analytical raw data generated during the chemical analysis of finished drug product, the raw material (API-Active.
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
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.
Calibration
Checklist / Formats
GLP
QC Sop
SOPs
- January 4, 2020
- by admin
Operation and Calibration of Analytical Balance
Standard Operating Procedure (SOP) for operation and calibration of analytical balances. As per USP, balance calibration parameters are Internal adjustments,.
