FDA Launching Single-Trial Pathway For In-Born Error Treatments, Called “RDEP”; Sponsors, Agency Will Agree Up-Front On “Supportive Evidence” Plan

You must be a logged-in member of this site to view this article.

To request more information about a company license to the Prevision Policy continuous information service or to get further details about the services we offer, please click here.

Alternatively, if your organization already has a license and you do not yet have an account, please click here to request access.