Abstract

The International Conference on Harmonization (ICH) Tripartite Guideline “Stability Testing of New Drug Substances and Products” sets out the stability testing requirements for a registration application within the three areas of the European Union, Japan, and the United States. These areas are assigned to climatic zone II with the storage condition of 25°C/60% RH. This paper describes the adjustments that are necessary to extend the guideline to countries of climatic zones III and IV.At first storage conditions were derived with 30°C/35% RH for climatic zone III and 30°C/70% RH for climatic zone IV. Both conditions contain a margin of safety compared to calculated and measured data in warehouses. Furthermore, they cover the extreme temperatures above 30 and 40°C which may arise in these climatic zones. Six months at 40°C/75% RH was fixed as storage condition for accelerated testing to assess organoleptic and physicochemical test criteria and to make predictions for chemical stability. The predictive factor is 3.3 for 30°C (6 months at 40°C corresponds to 20 months at 30°C). Extreme temperatures which may arise during shipment are covered by the results of stress investigations (e.g., 3 months at 50°C.The next adjustment is necessary for the selection of the packaging containers. They must reflect the requirements for solid, semisolid, and liquid dosage forms caused by the two storage conditions. In the evaluation the temperature difference of 10°C (40–30°C) instead of 15°C has to be considered, which limits the preliminary shelf lives in critical cases to 18 months instead of 24 months. Finally, statement/labeling must reflect the storage conditions. All of the other basic principles for the drug substances and drug products, such as selection and number of batches, test criteria, test procedures, specifications, testing frequency, and storage period can be applied without any change.

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