The Ultimate Resource for Pharmaceutical SOPs and Best Practices
In-process testing plays a pivotal role in pharmaceutical manufacturing, ensuring the quality, safety, and efficacy of pharmaceutical products. By conducting various tests throughout the manufacturing process, manufacturers can monitor critical parameters and identify any deviations or issues early on. In-process testing allows for real-time monitoring of key quality attributes such as content uniformity, dissolution rates, and microbiological purity, among others. This proactive approach helps to prevent defects, minimize batch failures, and ensure that products consistently meet regulatory requirements and quality standards. Moreover, in-process testing enables manufacturers to implement corrective actions promptly, improving process efficiency and reducing the risk of producing substandard or unsafe products. Ultimately, the importance of in-process testing in pharmaceuticals lies in its ability to uphold product quality, safeguard patient health, and maintain the integrity of the pharmaceutical industry as a whole.
SOP for Particulate Matter Testing in Liquids Procedure for Particulate Matter Testing in Liquids 1) Purpose The purpose of this SOP is to outline the procedure for testing particulate matter in liquid samples used in pharmaceutical manufacturing to ensure product quality and safety. 2) Scope This SOP applies to all liquid formulations produced within the…
SOP for Specific Gravity Testing of Liquids Procedure for Specific Gravity Testing of Liquids 1) Purpose The purpose of this SOP is to outline the procedure for measuring the specific gravity of liquid samples used in pharmaceutical manufacturing to ensure accurate density determination. 2) Scope This SOP applies to all liquid formulations produced within the…
SOP for Viscosity Testing of Liquids Procedure for Viscosity Testing of Liquids 1) Purpose The purpose of this SOP is to outline the procedure for measuring the viscosity of liquid samples used in pharmaceutical manufacturing to ensure consistency and quality control. 2) Scope This SOP applies to all liquid formulations produced within the manufacturing facility…
SOP for pH Measurement of Solutions Procedure for pH Measurement of Solutions 1) Purpose The purpose of this SOP is to outline the procedure for accurately measuring the pH of solutions used in pharmaceutical manufacturing to ensure consistency and quality. 2) Scope This SOP applies to all solutions used within the manufacturing facility that require…
SOP for Uniformity of Dosage Units Procedure for Uniformity of Dosage Units Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the uniformity of dosage units (tablets) to ensure consistent distribution of the active pharmaceutical ingredient (API) among individual units. 2) Scope This SOP applies to all batches of…
SOP for Capsule Dissolution Testing Procedure for Capsule Dissolution Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the dissolution of capsules to ensure consistent release of the active pharmaceutical ingredient (API) over a specified time period. 2) Scope This SOP applies to all capsule batches produced within the…
SOP for Capsule Disintegration Testing Procedure for Capsule Disintegration Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the disintegration of capsules to ensure they break down into smaller particles or dissolve completely within the specified time frame for effective drug release. 2) Scope This SOP applies to all…
SOP for Capsule Content Uniformity Procedure for Capsule Content Uniformity Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the content uniformity of capsules to ensure consistent distribution of active pharmaceutical ingredient (API) across all dosage units. 2) Scope This SOP applies to all capsule batches produced within the…
SOP for Capsule Weight Variation Procedure for Capsule Weight Variation Testing 1) Purpose The purpose of this SOP is to outline the procedure for determining the weight variation of capsules to ensure uniformity and compliance with pharmacopeial standards. 2) Scope This SOP applies to all capsule batches produced within the manufacturing facility. 3) Responsibilities Quality…
SOP for Tablet Dissolution Testing Procedure for Tablet Dissolution Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the dissolution of tablets to ensure consistent release of the active pharmaceutical ingredient (API) over a specified time period. 2) Scope This SOP applies to all tablet batches produced within the…