The Ultimate Resource for Pharmaceutical SOPs and Best Practices
Standard Operating Procedure (SOP) for Operation of Tablet Deduster Purpose The purpose of this SOP is to provide guidelines for the safe and efficient operation of the tablet deduster in pharmaceutical manufacturing. It ensures the removal of dust and excess particles from tablets, maintaining product quality and compliance with regulatory standards. Scope This SOP applies…
Standard Operating Procedure (SOP) for Cleaning & Maintenance of Sieving Equipment 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the effective cleaning and maintenance of sieving equipment in order to ensure optimal performance, prevent contamination, and maintain the quality of pharmaceutical products. 2. Scope This SOP applies to…
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Standard Operating Procedure (SOP) for Sieve Replacement and Calibration 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper replacement and calibration of sieves used in pharmaceutical manufacturing, ensuring accurate particle size analysis and maintaining product quality. 2. Scope This SOP applies to all personnel involved in the…
Standard Operating Procedure for Water Testing SOP Version: 1.0 Purpose: The purpose of this Standard Operating Procedure (SOP) is to establish guidelines and procedures for water testing in the pharmaceutical manufacturing facility. Water testing is performed to assess the microbiological quality and purity of water used in various manufacturing processes, in compliance with relevant pharmacopeias…
Standard Operating Procedure (SOP) for Operation of Sieving Machine 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the safe and efficient operation of the sieving machine in order to maintain the quality and integrity of pharmaceutical products. 2. Scope This SOP applies to all personnel involved in operating…
Standard Operating Procedure for Bioburden Testing SOP Version: 1.0 Purpose: The purpose of this Standard Operating Procedure (SOP) is to establish guidelines and procedures for bioburden testing in the pharmaceutical manufacturing facility. Bioburden testing is performed to determine the level of viable microorganisms present in raw materials, intermediate products, or finished pharmaceutical products, in compliance…
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Standard Operating Procedure (SOP) for Sieving Process and Sieve Inspection 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for the sieving process and sieve inspection in order to ensure the quality and integrity of pharmaceutical products. 2. Scope This SOP applies to all personnel involved in the sieving process…
Standard Operating Procedure (SOP) for Regulatory Submission Process Purpose: The purpose of this SOP is to establish a standardized process for the regulatory submission of documents and data to health authorities, ensuring compliance with applicable regulations and guidelines. Scope: This SOP applies to all personnel involved in the regulatory submission process within the organization. Responsibilities:…
1. Purpose: The purpose of this SOP is to provide a systematic approach to the regulatory submission process within our organization. 2. Scope: This SOP applies to all employees involved in the regulatory submission process, including but not limited to regulatory affairs personnel, project managers, clinical operations personnel, and quality assurance personnel. 3. Responsibilities: The…
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Standard Operating Procedure for Microbial Limit Testing SOP Version: 1.0 Purpose: The purpose of this Standard Operating Procedure (SOP) is to establish guidelines and procedures for microbial limit testing in the pharmaceutical manufacturing facility. Microbial limit testing is performed to determine the microbial load in pharmaceutical products or raw materials, ensuring compliance with relevant pharmacopeial…
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