Pharma Stability: Insights, Guidelines, and Expertise
Selection and Management of Container-Liner-Closure Systems Purpose The purpose of this Standard Operating Procedure (SOP) is to outline the procedures for selecting and managing container-liner-closure systems used in stability studies. This ensures that the packaging systems protect the integrity and quality of the drug product throughout the stability study. Scope This SOP applies to all…
Qualification and Certification of Container-Liner-Closure Systems for Stability Studies Purpose The purpose of this Standard Operating Procedure (SOP) is to outline the procedures for the certification of container-liner-closure systems used in stability studies. This ensures that the packaging systems are qualified and certified to maintain the integrity and quality of the drug product throughout the…
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Documentation and Reporting of Stability Study Test Results Purpose The purpose of this Standard Operating Procedure (SOP) is to describe the process for documenting and reporting the test results of stability studies. This ensures that the data is accurately recorded, analyzed, and communicated in a standardized format for regulatory compliance and decision-making. Scope This SOP…
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Management of Abnormal and OOS Results in Stability Studies Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for identifying, investigating, and managing abnormal or out-of-specification (OOS) results observed during stability studies. This ensures that all OOS results are handled in a consistent, documented, and compliant manner. Scope This SOP…
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Management of Stability Chamber Malfunctions and Storage Condition Deviations Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for managing and resolving stability chamber breakdowns or deviations from specified storage conditions during stability studies. This ensures the integrity of the study is maintained and that corrective actions are taken promptly….
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Documentation of Climatic Conditions for Stability Studies Purpose The purpose of this Standard Operating Procedure (SOP) is to establish the process for accurately recording and documenting the climatic conditions (temperature, humidity, etc.) during stability studies. This ensures that the environmental conditions are consistently monitored and reported, maintaining the integrity of the stability data. Scope This…
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Monitoring and Management of Temperature and Humidity Records Purpose The purpose of this Standard Operating Procedure (SOP) is to establish the process for reviewing and controlling temperature and humidity recording charts used in stability studies. This ensures that environmental conditions are consistently monitored, recorded accurately, and deviations are promptly addressed to maintain the integrity of…
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Revalidation Procedure for Stability Chambers Purpose The purpose of this Standard Operating Procedure (SOP) is to outline the process for the periodic revalidation of climatic rooms and chambers used in stability studies. This ensures that these environments consistently meet specified conditions and maintain the integrity of the stability data. Scope This SOP applies to all…
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Cleaning and Maintenance of Stability Chambers Purpose The purpose of this Standard Operating Procedure (SOP) is to establish the sanitation and housekeeping requirements for climatic chambers used in stability studies. This ensures that the chambers are maintained in a clean and orderly condition, preventing contamination and ensuring accurate stability data. Scope This SOP applies to…
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Photostability Testing Procedure Purpose The purpose of this Standard Operating Procedure (SOP) is to establish the procedures for conducting photostability studies on drug substances and drug products. This ensures that the products are tested under controlled light conditions to determine their stability when exposed to light. Scope This SOP applies to all drug substances and…