Non-clinical documentation for mixed marketing authorisation applications

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Current effective version

Adopted guideline

Reference numberCPMP/SWP/799/95
Effective from30/04/2006
KeywordsMixed marketing authorisation application, documentation, non-clinical
DescriptionThis document aims to give advice to applicants who plan to submit a mixed marketing authorisation application for medicinal products for human use. It applies to conventional chemical active substances of defined structure.

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