What is an IMPD, and when is it required?

1 company with a published answer

  1. MultiHealth group

    “The IMPD (Investigational Medicinal Product Dossier) is the regulatory dossier describing the quality, manufacturing, and preclinical/clinical data for an investigational drug. It is required upon the initial submission of a clinical trial through the CTIS.”

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Surface ID
urn:readyscan:corpus:buyer-question:multihealth-group-q115036354-answer-8ac688cc89dfe257172b
Material fingerprint
fnv1a64:c4dd1ba84248849f
Membership fingerprint
fnv1a64:13eda3f164d7874f
Published
2026-10-29
Modified
2026-10-29
ready-scan-subjects/Q115036354
revision Q115036354:content:bf641adcdb087deb

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