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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CO COA COB COC COD COE COF COG COH COI COK COL COM CON COO COP COQ COR COS COT COU COV COW COX COY COZ

Consent Form

[A document explaining all relevant study information to assist the study volunteer in understanding the expectations and requirements of participation in a clinical trial. This document is presented to and signed by the study subject. (from centerwatch.com glossary) ( NCI )]
UMLS (NCI) C0009797
 
Intellectual Product
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