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cGMP QA Sop Quality Control SOPs Stores Sops

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

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cGMP Checklist Checklist / Formats Production Production Sop QA Sop

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

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cGMP Health & Safety (EHS) Maintenance Sops Micro Sop QA Sop QC Sop SOPs Validation

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).

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Calibration cGMP GLP QC Sop Quality Control SOPs

Auto Titrator – Operation and Calibration SOP

Standard Operating Procedure (SO) for Operation and Calibration of Auto Titrator (Potentiometer) for its utility in carrying out different types

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cGMP GLP Health & Safety (EHS) Production Production Sop QA Sop QC Sop Quality Control SOPs

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

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cGMP Checklist / Formats Protocol QA Sop SOPs Validation

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.

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cGMP Checklist / Formats GLP QA Sop SOPs

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

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cGMP Micro Sop Microbiology SOPs

Refrigerator – Operation & Performance Check

Standard Operating Procedure (SOP) for Operation, Cleaning, and Performance Check for Refrigerator used to store the  Microbiology Culture, Spores, Media,

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cGMP Checklist Checklist / Formats Environment Health & Safety (EHS) Production Production Sop QA Sop QC Sop SOPs Validation

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

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Calibration cGMP Checklist / Formats GLP HPLC QC Sop Quality Control SOPs

UPLC System Calibration Procedure

Calibration Procedure / SOP for Ultra Performance Liquid Chromatography (UPLC) System. UPLC can be regarded as a new direction for

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