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Quality Assurance SOP

Following are the useful SOPs, helpful to new as well as experienced professionals in quality improvement of products. They play a very vital role in every industries. SOPs are a set of policies, standards, and procedures the organization needs in the management and operations of the entire organization to ensure success.
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SOP for Document Control System

SOP for In-process Sampling and Analysis of Oral Drug Products

SOP for Reprocessing of Out of Specification Batch

SOP for Handling of Customer Complaints

SOP for Quality Management Documents Numbering System

SOP for Quality Risk Management Plan

SOP for Handling of Rejected Batches

SOP for Quality Assurance Department

SOP for Laundry in Pharmaceuticals

SOP for Prevention of Product Mix-ups and Cross-Contamination

SOP for Preparation of Certificate of Analysis

SOP for Password for Computers and Software in Pharmaceutical

SOP for Preparation of Master Formula Record (MFR)

SOP for Batch Numbering System

SOP for Handling of Waste Paper In Pharmaceutical Industry

SOP for Destruction of Analytical Samples After Testing

SOP for Supplier Qualification

SOP for Document distribution, Control, Storage and Disposal procedure

SOP for Handling of Incident in Pharmaceuticals

SOP for Allocation of Identification Numbers to Instruments / Equipments

SOP for Usage of Personal Protective Equipment

SOP for Handling of Scrap in Pharmaceuticals

SOP for General Housekeeping

SOP for Calibration Programme

SOP for Log Book Preparation

SOP for Numbering System of Analytical Report Number

SOP for Corrective Action and Preventive Action (CAPA)

SOP for Induction Program and Training of Personnel

SOP for In-process Monitoring and Control

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

SOP for Job Responsibility

SOP for Handling Out of Specification (OOS)

SOP for Change Control in Pharmaceuticals

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

SOP for Entry, Exit in production & Quality Control Area

SOP for Product Recall

SOP for Rework/Reprocessing Procedure

SOP for Internal Audit

SOP for Vendor Qualification and Management

SOP for Dose Solubility Volume Ratio of Active Pharmaceutical Ingredients

SOP for Handling of Out of Trend (OOT)

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

SOP for Data Integrity

SOP for Annual Product Review (APR)

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