News by Tag: Fda Ind Application
RAPS pre-approved webinar on "The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content "
September 21, 2012
:"The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations" is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel will organize on November 8.
September 21, 2012
:"The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations" is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel will organize on November 8.