FDA Wants Clinical Endpoints – Not Surrogates – In Alpha-1 Pre-Registration Studies, But Can Be Flexible On P-Values
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.
OR