FDA lacks comprehensive data to determine whether risk evaluation and mitigation strategies improve drug safety.

Author/creator United States
Format Electronic
Publication[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2013.
Description1 online resource (34 pages) : illustrations
Supplemental Contenthttps://purl.fdlp.gov/GPO/gpo68938
Subjects

Variant title Food and Drug Administration lacks comprehensive data to determine whether risk evaluation and mitigation strategies improve drug safety
Variant title Running title: FDA lacks comprehensive data to determine whether REMS improve drug safety
General noteTitle from title screen (viewed June 13, 2016).
General note"February 2013."
General note"OEI-04-11-00510."
General noteGPO Cataloging Record Distribution Program (CRDP).
Bibliography noteIncludes bibliographical references.
Technical rpt numberOEI-04-11-00510
GPO item number0445-B-07 (online)
Govt. docs number HE 1.75:OEI-04-11-00510

Availability

Library Location Call Number Status Item Actions
Electronic Resources Access Content Online ✔ Available