Tag: FDA Stability Testing Requirements

ICH Stability Storage Conditions: Designing Effective Programs

ICH Stability Storage Conditions: Designing Effective Programs Step-by-Step Guide to Designing Stability Programs with ICH Storage Conditions Introduction Stability testing is a cornerstone of pharmaceutical development, ensuring that products maintain their quality, safety, and efficacy over time. The International Council for Harmonisation (ICH) provides a globally accepted framework for stability testing, including specific storage conditions…

Regulatory Guidelines

SOP for Assessing the Stability of Chiral Drugs

SOP for Assessing the Stability of Chiral Drugs Guidelines for Stability Testing of Chiral Drugs 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on chiral drugs. Stability testing ensures that chiral drugs maintain their stereochemistry, safety, efficacy, and quality throughout their shelf life under various storage…

Stability Studies SOP

Understanding ICH Q1C: Stability Testing of New Dosage Forms

Understanding ICH Q1C: Stability Testing of New Dosage Forms Step-by-Step Guide to ICH Q1C: Stability Testing of New Dosage Forms Introduction Stability testing is a critical component of pharmaceutical development, ensuring that drug products maintain their quality, safety, and efficacy over time. While ICH Q1A(R2) provides a framework for stability studies of new drug substances…

Regulatory Guidelines

Adapting Stability Testing Programs for Multinational Compliance

Adapting Stability Testing Programs for Multinational Compliance Tips for Adapting Stability Testing Programs for Multinational Compliance Introduction Pharmaceutical manufacturers operating in global markets must navigate a maze of regulatory requirements for stability testing. While frameworks like the ICH Q1A(R2) provide harmonized guidelines, regional agencies such as the FDA, EMA, and ASEAN introduce unique conditions and…

Regulatory Guidelines

SOP for Performing Stability Studies for Freeze-Dried Products

SOP for Performing Stability Studies for Freeze-Dried Products Guidelines for Stability Testing of Freeze-Dried (Lyophilized) Products 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on freeze-dried (lyophilized) products. Stability testing is essential to ensure that these products maintain their safety, efficacy, and quality throughout their shelf…

Stability Studies SOP

ASEAN Guidelines for Stability Studies in Tropical Climates

ASEAN Guidelines for Stability Studies in Tropical Climates Understanding ASEAN Guidelines for Stability Studies in Tropical Climates Introduction The ASEAN Stability Guidelines provide a tailored framework for conducting stability studies in tropical climates, addressing the unique environmental challenges of the Southeast Asian region. High temperatures and humidity levels can significantly affect the stability of pharmaceutical…

Regulatory Guidelines

EMA Shelf-Life Guidelines: Navigating Regulatory Challenges

EMA Shelf-Life Guidelines: Navigating Regulatory Challenges Expert Guide to EMA Shelf-Life Guidelines: Overcoming Regulatory Challenges Introduction Shelf life is a critical attribute of pharmaceutical products, ensuring their quality, safety, and efficacy over time. In the European market, the European Medicines Agency (EMA) governs shelf-life determination through stringent guidelines aligned with international standards like ICH Q1A(R2)….

Regulatory Guidelines

SOP for Conducting Stability Studies for Low-Dose Formulations

SOP for Conducting Stability Studies for Low-Dose Formulations Guidelines for Stability Testing of Low-Dose Formulations 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on low-dose formulations. Stability testing ensures that these formulations maintain their safety, efficacy, and quality throughout their shelf life under various storage conditions….

Stability Studies SOP

ICH Q1B for Photostability Testing: Ensuring Drug Safety

ICH Q1B for Photostability Testing: Ensuring Drug Safety Step-by-Step Guide to ICH Q1B: Photostability Testing for Drug Safety Introduction Photostability testing is a critical aspect of pharmaceutical development, ensuring that drug products remain stable and effective when exposed to light. The ICH Q1B guideline provides a comprehensive framework for evaluating the effects of light exposure…

Regulatory Guidelines

SOP for Assessing Stability for Polymorphic Drugs

SOP for Assessing Stability for Polymorphic Drugs Guidelines for Stability Testing of Polymorphic Drugs 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on polymorphic drugs. Stability testing ensures that the drug’s polymorphic form remains stable and does not undergo any undesired changes under various storage conditions…

Stability Studies SOP