SOP for Environmental Monitoring Program Standard Operating Procedure for Environmental Monitoring Program 1) Purpose This SOP outlines the procedures for conducting an environmental monitoring program to ensure that the manufacturing environment meets the required cleanliness and microbiological standards, ensuring the quality and safety of pharmaceutical products. 2) Scope This SOP applies to all areas within…
Out-of-Specification SOP
SOP for Microbiological Quality Assurance
SOP for Microbiological Quality Assurance Standard Operating Procedure for Microbiological Quality Assurance 1) Purpose This SOP outlines the procedures for ensuring microbiological quality assurance of pharmaceutical products to maintain their safety, efficacy, and compliance with regulatory standards. 2) Scope This SOP applies to all microbiological testing activities carried out on raw materials, in-process samples, finished…
Quality Assurance: SOP for Environmental Monitoring Program
SOP for Environmental Monitoring Program Standard Operating Procedure for Environmental Monitoring Program 1) Purpose This SOP outlines the procedures for conducting an environmental monitoring program to ensure that the manufacturing environment meets the required cleanliness and microbiological standards, ensuring the quality and safety of pharmaceutical products. 2) Scope This SOP applies to all areas within…
SOP for Sampling Procedures
SOP for Sampling Procedures Standard Operating Procedure for Sampling Procedures 1) Purpose This SOP outlines the procedures for sampling raw materials, intermediates, active pharmaceutical ingredients (APIs), and finished products to ensure that samples are representative and suitable for testing and analysis. 2) Scope This SOP applies to all sampling activities conducted within the pharmaceutical manufacturing,…
SOP for Stability Studies
SOP for Stability Studies Standard Operating Procedure for Stability Studies 1) Purpose This SOP outlines the procedures for conducting stability studies on pharmaceutical products to determine their shelf life and ensure that they maintain their intended quality, safety, and efficacy throughout their storage period. 2) Scope This SOP applies to all pharmaceutical products, including drug…
SOP for Stability Data Management
SOP for Stability Data Management Standard Operating Procedure for Stability Data Management 1) Purpose This SOP outlines the procedures for managing stability data generated from stability studies to ensure accurate documentation, analysis, and reporting of data to support product shelf life and regulatory submissions. 2) Scope This SOP applies to all stability data generated from…
SOP for Analytical Method Validation
SOP for Analytical Method Validation Standard Operating Procedure for Analytical Method Validation 1) Purpose This SOP outlines the procedures for validating analytical methods used in the testing of pharmaceutical products to ensure their accuracy, precision, specificity, robustness, and compliance with regulatory requirements. 2) Scope This SOP applies to all analytical methods used for the testing…
SOP for Computer System Validation
SOP for Computer System Validation Standard Operating Procedure for Computer System Validation 1) Purpose This SOP outlines the procedures for validating computer systems used in pharmaceutical manufacturing, testing, control, and documentation processes to ensure data integrity, reliability, and compliance with regulatory requirements. 2) Scope This SOP applies to all computerized systems that manage or control…
SOP for Equipment Qualification (IQ/OQ/PQ)
SOP for Equipment Qualification (IQ/OQ/PQ) Standard Operating Procedure for Equipment Qualification (IQ/OQ/PQ) 1) Purpose This SOP outlines the procedures for Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of equipment to ensure that equipment is properly installed, operates as intended, and consistently produces results meeting predefined specifications. 2) Scope This SOP applies to…
Quality Assurance: SOP for Cleaning Validation
SOP for Cleaning Validation Standard Operating Procedure for Cleaning Validation 1) Purpose This SOP outlines the procedures for conducting cleaning validation studies to ensure that cleaning procedures effectively remove residues of products, cleaning agents, and microbial contaminants from equipment surfaces to prevent cross-contamination and ensure product quality and safety. 2) Scope This SOP applies to…