IMPD/eIMPD

The first step towards eCTD

Under European law you require an IMPD before commencing a clinical trial in man. By adopting the right eIMDP concept you can create part of your marketing authorisation dossier in eCTD format already at an early stage. In so doing you will profit from the close collaboration with our Pharmaceutical Quality, Preclinical, Clinical and eSubmission Management departments. We are your single point of contact for in-depth advice and dossier management in connection with your eIMPDs.