|
FDA Rolls Out New eCTD Docs for Sponsors, Offers Grants for Orphan Drug Trials
Drugmakers can now access final versions of documents related to the FDA’s major update of the electronic Common Technical Document (eCTD), but industry shouldn’t expect to make regulatory submissions using the new electronic format for at least a year.
This article is viewable by subscribers only. To view this article, please select an option below.
|
|
Subscribe
Archives