| FDAAA 801 Requirement (Clinical trial registration mandatory)|
FDAAA 801 Requirements "This page provides summary information on the clinical trial registration and results submission requirements described in Section 801 of the Food and Drug Administration Amendments Act (PDF), known as FDAAA 801. It includes information about the Responsible Party, Applicable Clinical Trials, deadlines for submitting required information, and penalties."
| Future cancer research priorities in the US (2017)|
Collection published in The Lancet
* Regional pages of relevance for your country: Americas
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