SOP for Quality Assurance

The following are useful SOPs that are helpful to new and experienced professionals in the quality improvement of products. They play a very vital role in every industry. SOPs are a set of policies, standards, and procedures the organization needs to manage and operate the entire organization to ensure success. This site is updated regularly, so visit again and share it.

SOP of Release or Rejection of Finished Product

SOP for Batch Release for Finished Goods

SOP for Standard Operating Procedure in Pharmaceutical

SOP for Job Responsibility

SOP for Preparation of Site Master File

SOP for Handling of Waste Paper in the Pharmaceutical Industry

SOP for Job Responsibility of Quality Assurance Personnel

SOP for Annual Product Quality Review

SOP for Internal Audit Plan as per GMP

SOP for Procedure for Making Corrections in Documents

SOP for Qualification of Analyst

SOP for Out of Acceptance Limit in Purified Water System

SOP for General Housekeeping

SOP for Sampling & Handling of Semi-Finished & Finished Products

SOP for Entry, Exit in production & Quality Control Area

SOP for Preparation and Issuance of Data Sheet

SOP for Usage of Personal Protective Equipment

SOP for Logbook Preparation

SOP for Calibration Programme

SOP for Issue, Entry, Review and Control of Batch Manufacturing Records

SOP for Password for Computers and Software in Pharmaceutical

SOP for Product Traceability and retrieval (Mock Recall)

SOP for Product Recall

SOP for Preparation, Approval, Issue and Control of Work Sheets for Record of Analysis

SOP for Vendor Qualification and Approval

SOP for Checking the Correctness of Computerized Formulation Order Issue System

SOP for Handling of Scrap in Pharmaceuticals

SOP for Production Activities as per Safety & cGMP Requirement

SOP for Password, Data Backup and Storage for Computer System

SOP for Numbering System of Analytical Report Number

SOP for Allocation of Identification Numbers to Instruments/Equipment

SOP for Signature Registration of Employees
SOP for Prevention of Product Mix-ups and Cross-Contamination

SOP for In-process Monitoring and Control

SOP for Destruction of Analytical Samples After Testing

SOP for Quality Assurance Department

SOP for Batch Numbering System

SOP for Quality Management Documents Numbering System

SOP for Quality Risk Assessment and Quality Risk Management (QRM)

SOP for Reprocessing of Out of Specification Batch

SOP for Assigning Manufacturing & Expiry Date/Retesting Date

SOP for Handling of Rejected Batches

SOP for Handling of Returned Material/Products

SOP for Quality Risk Management Plan

SOP for Supplier Qualification

SOP for Corrective Action and Preventive Action (CAPA)

SOP for Document distribution, Control, Storage and Disposal procedure

SOP for Handling of Incidents in Pharmaceuticals

SOP for Internal Audit

SOP for Preparation of Master Formula Record (MFR)

SOP for Document Control, Issuance and Numbering System

SOP for Review of Electronic Audit Trail

SOP for Handling of Out of Calibration

SOP for Quality Risk Management

SOP for Change Control in Pharmaceuticals

SOP for Vendor Qualification and Management

SOP for Handling of Deviation

SOP for Rework/Reprocessing Procedure

SOP for Data Integrity

SOP for Handling of Out of Trend (OOT)
SOP for Handling Out of Specification (OOS)
SOP for Preparation of Certificate of Analysis (COA)
SOP for Approval and Release of Finished Goods
SOP for Document Control
SOP for Temperature Mapping of Warehouse
SOP for Handling of Customer Complaints
SOP for Audit Trail Review
SOP for Review and Approval of Analytical Raw Data
SOP for Complaint Handling Process
SOP for Quality Management System
SOP for Analytical Data Review