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Guideline on Stability Testing for Active and Medicinal Products Manufactured in Climatic Zones III and IV to be Marketed in the EU - Explanatory Note on the Withdrawal of ICH Q1F

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CPMP Guideline
The ICH guideline Q1F was intended to define the type and extent of stability studies required in those cases, where parts of the manufacture of the active substance or drug product were performed in climatic zone III and IV. In the meantime this guideline has been withdrawn.

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