The Ultimate Resource for Pharmaceutical SOPs and Best Practices
SOP for UV Exposure Testing Procedure for UV Exposure Testing 1) Purpose The purpose of this SOP is to outline the procedure for conducting UV exposure testing on pharmaceutical products to assess the impact of UV radiation on product stability and quality. 2) Scope This SOP applies to all pharmaceutical products susceptible to degradation from…
SOP for Light Exposure Testing Procedure for Light Exposure Testing 1) Purpose The purpose of this SOP is to outline the procedure for conducting light exposure testing on pharmaceutical products to assess the potential impact of light exposure on product stability and quality. 2) Scope This SOP applies to all pharmaceutical products susceptible to degradation…
SOP for Humidity Mapping of Storage Areas Procedure for Humidity Mapping of Storage Areas 1) Purpose The purpose of this SOP is to outline the procedure for conducting humidity mapping studies in storage areas to ensure uniformity and stability of humidity conditions for stored pharmaceutical products. 2) Scope This SOP applies to all storage areas…
SOP for Temperature Mapping of Storage Areas Procedure for Temperature Mapping of Storage Areas 1) Purpose The purpose of this SOP is to outline the procedure for conducting temperature mapping studies in storage areas to ensure uniformity and stability of temperature conditions for stored pharmaceutical products. 2) Scope This SOP applies to all storage areas…
SOP for Particle Count Testing in Cleanrooms Procedure for Particle Count Testing in Cleanrooms 1) Purpose The purpose of this SOP is to outline the procedure for conducting particle count testing in cleanrooms to monitor airborne particulate levels and ensure compliance with specified cleanliness standards. 2) Scope This SOP applies to all cleanrooms and controlled…
SOP for Airflow Visualization Studies Procedure for Airflow Visualization Studies 1) Purpose The purpose of this SOP is to outline the procedure for conducting airflow visualization studies in cleanrooms to assess and validate the effectiveness of airflows in maintaining specified cleanliness levels. 2) Scope This SOP applies to all cleanrooms and controlled environments within the…
SOP for Clean Steam Quality Testing Procedure for Clean Steam Quality Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the quality of clean steam used in pharmaceutical manufacturing processes to ensure it meets specified standards for purity and suitability. 2) Scope This SOP applies to all stages of…
SOP for Water for Injection (WFI) Quality Testing Procedure for Water for Injection (WFI) Quality Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the quality of Water for Injection (WFI) used in pharmaceutical manufacturing to ensure it meets specified standards for purity and suitability. 2) Scope This SOP…
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SOP for Compressed Air Quality Testing Procedure for Compressed Air Quality Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the quality of compressed air used in pharmaceutical manufacturing to ensure it meets specified standards for purity and cleanliness. 2) Scope This SOP applies to all areas within the…
SOP for Environmental Monitoring in Cleanrooms Procedure for Environmental Monitoring in Cleanrooms 1) Purpose The purpose of this SOP is to outline the procedure for conducting environmental monitoring in cleanrooms to assess air quality and microbial contamination levels. 2) Scope This SOP applies to all cleanrooms within the facility where pharmaceutical products are manufactured, requiring…
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