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Protocol Representation Sub-Domain
The Protocol Representation sub-domain is intended for those involved in the planning and design of a research protocol. The majority of business requirements have come from those involved in clinical trial protocols. It focuses on the characteristics of a study and the definition and association of activities within the protocols, including "arms" and "epochs". It also includes the definitions of the roles that participate in those activities. (NCI Thesaurus)
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A protocol was misinterpreted.
Occurrences within some epochs that are initiated by a protocol-specified event. The most common protocol milestone is "Informed Consent Obtained" which usually…
Primary clinical researcher of a clinical trial, ultimately responsible for all aspects in the conduct of a study, but has special responsibility…
An office within NCI which provides administrative support for clinical trial development and tracking by abstraction of key elements into a web-based…
The description and the values of the components comprising Case Report forms.
Protocols, with Case Report Forms included, stipulate the execution of Clinical Trials.
