The Ultimate Resource for Pharmaceutical SOPs and Best Practices
Standard Operating Procedure for Batch Release and Product Release 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the systematic and controlled process of batch release and product release in the pharmaceutical manufacturing facility. This SOP ensures that each batch of pharmaceutical products undergoes thorough review, testing, and verification…
Standard Operating Procedure for Batch Record Preparation and Documentation 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper preparation and documentation of batch records in the pharmaceutical manufacturing process. This SOP ensures that batch records are accurately and comprehensively documented, reflecting all critical steps, measurements, and observations…
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Standard Operating Procedure for Equipment Verification and Calibration 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the verification and calibration of equipment used in the pharmaceutical manufacturing process. This SOP ensures that all equipment is regularly checked for accuracy, precision, and compliance with required specifications to maintain the…
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Standard Operating Procedure for Handling and Transporting Tablets within the Department 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for the safe and proper handling and transportation of tablets within the manufacturing department. This SOP aims to minimize the risk of tablet damage, contamination, and mix-up during handling and…
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Standard Operating Procedure for Inventory Control and Stock Rotation 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for the effective inventory control and stock rotation of pharmaceutical products within the manufacturing facility. This SOP aims to ensure that the oldest stock is used first (first-in-first-out, FIFO), minimize product expiry,…
Standard Operating Procedure for Tablet Storage and Retrieval 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper storage, organization, and retrieval of tablets in the pharmaceutical manufacturing facility. This SOP ensures that tablets are stored under controlled conditions, easily accessible, and that the correct inventory is maintained…
Standard Operating Procedure for Operation of Tablet Storage and Handling Equipment 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper operation and handling of tablet storage equipment to ensure the storage conditions meet the required specifications, prevent contamination, and maintain the quality of the tablets during storage….
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Standard Operating Procedure for Handling and Rejection of Defective Tablets 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper handling and rejection of defective tablets identified during the manufacturing or inspection process. This SOP ensures that defective tablets are segregated, properly disposed of, and that appropriate actions…
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Standard Operating Procedure for Cleaning and Maintenance of Inspection Equipment 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for the systematic cleaning and maintenance of inspection equipment to ensure its accuracy, reliability, and optimal performance during quality control activities. This SOP aims to prevent contamination, reduce downtime, and extend…
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Standard Operating Procedure for Tablet Inspection Process 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide detailed guidelines for the systematic and controlled inspection of tablets to ensure their quality, integrity, and compliance with specifications. This SOP aims to identify and eliminate any defective tablets before packaging and distribution. 2. Scope…