Pharma Stability: Insights, Guidelines, and Expertise
How to Implement Stability Testing for Veterinary Drugs as per US FDA and EMA Guidelines Stability Testing for Veterinary Drugs: Compliance with FDA and EMA Guidelines Introduction Veterinary drugs, like human pharmaceuticals, require stability testing to ensure they maintain their quality, safety, and efficacy throughout their shelf life. The US FDA and the EMA provide…
How to Apply Stability Testing Guidelines for New Drug Submissions to EMA Stability Testing for New Drug Submissions: Compliance with EMA Guidelines Introduction New drug submissions to the European Medicines Agency (EMA) require comprehensive stability testing to demonstrate that the drug product will maintain its quality, safety, and efficacy over its shelf life. The EMA…
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How to Conduct Stability Testing for Sterile Products as per Regulatory Requirements Stability Testing for Sterile Products: Compliance with Regulatory Standards Introduction Sterile products, including injectables, ophthalmic solutions, and other aseptically processed products, require stringent stability testing to ensure they remain sterile, safe, and effective throughout their shelf life. Regulatory authorities such as the US…
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SOP for Evaluating the Impact of Light Exposure on Drug Products Procedure for Assessing the Impact of Light Exposure on Drug Products 1) Purpose The purpose of this SOP is to provide a standardized procedure for evaluating the impact of light exposure on the stability of drug products. This assessment helps in determining suitable packaging…
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How to Address Stability Testing Requirements for Herbal Medicines per Regulatory Guidelines Stability Testing for Herbal Medicines: Meeting Regulatory Standards Introduction Herbal medicines, derived from plant materials, require specific stability testing to ensure their quality, safety, and efficacy over their shelf life. Regulatory authorities, such as the US FDA, EMA, and WHO, provide guidelines for…
How to Conduct Stability Testing as per ICH Q5C for Biotechnological/Biological Products Implementing ICH Q5C Guidelines for Stability Testing of Biological Products Introduction Biotechnological and biological products, such as monoclonal antibodies, therapeutic proteins, and vaccines, require specific stability testing to ensure they maintain their quality, safety, and efficacy throughout their shelf life. The ICH Q5C…
How to Conduct Stability Testing for Biotech Products in Compliance with US FDA Guidelines Stability Testing for Biotechnological Products: FDA Compliance Introduction Biotechnological products, such as monoclonal antibodies, recombinant proteins, and gene therapy products, require rigorous stability testing to ensure their quality, safety, and efficacy throughout their shelf life. The US FDA provides specific guidelines…
How to Implement Stability Testing for Temperature-Sensitive Products per ICH Q1A(R2) Stability Testing for Temperature-Sensitive Products: Applying ICH Q1A(R2) Guidelines Introduction Temperature-sensitive products, such as biological drugs, vaccines, and certain chemical compounds, require specialized stability testing to ensure they maintain their quality, safety, and efficacy throughout their shelf life. The ICH Q1A(R2) guidelines provide specific…
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How to Address Stability Testing Requirements for Pediatric Drug Products per Regulatory Guidelines Stability Testing for Pediatric Drug Products: Meeting Regulatory Requirements Introduction Pediatric drug products require specific stability testing to ensure they remain safe and effective for use in children throughout their shelf life. Regulatory authorities such as the US FDA, EMA, and Health…
How to Conduct Stability Studies for Generics in Compliance with US FDA Guidance Guidelines for Stability Testing of Generic Drugs as per US FDA Requirements Introduction Generic drugs must meet the same quality, safety, and efficacy standards as their branded counterparts. Stability studies are crucial for demonstrating that a generic product maintains these standards throughout…
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