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Audit Calibration cGMP GLP SOPs

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

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Audit Calibration GLP Quality Control SOPs

SOP for Internal and External Calibration of Instrument

Standard Operating Procedure for Laboratory Instrument and Equipment calibration through Internal or External (Third Party). This SOP includes the calibration

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Checklist Checklist / Formats Micro Sop Microbiology SOPs Sterile

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

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cGMP Checklist Production Production Sop QA Sop SOPs

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

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Audit Checklist Checklist / Formats Doc GC GLP HPLC

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

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cGMP Checklist / Formats Protocol QA Sop QC Sop Quality Control SOPs

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

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Calibration GLP QC Sop Quality Control SOPs

SOP for Operation and Calibration of UV Cabinet

Standard Operating Procedure for Operation and calibration of UV cabinet for reviewing the TLC plate, Photolytic Degradation, UV cabinet Performance

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Audit GLP QC Sop Quality Control SOPs

SOP for Audit Trail Review and Privilege Policy 

In the Quality Control Laboratory of the pharmaceutical product manufacturing unit, Different instruments, and equipment being used to analyze the

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cGMP Micro Sop Microbiology SOPs

Isolation and Identification of Microorganisms

Standard Operating Procedure (SOP) for Isolation and Identification of Microorganisms (Microbes). Isolation and Identification of Microorganisms 1.0      PURPOSE:

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cGMP Checklist / Formats QA Sop SOPs

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

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