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Tailor-made Dossiers for Your Products

On your behalf, we will develop tailor-made dossiers for your products. These are precisely tuned to your demands and comply with the current regulatory requirements. You will receive the dossier in the form of a common technical document (CTD), the mandatory format for all marketing authorisations and registration applications for pharmaceuticals since 2003. Ready for submission to the approval body – including all expert reports and with all five or just a few selected CTD modules, as you require. We will of course take into account special layout requests you may have.