| The Research
Database The NCR research
database includes individuals who have come to the research center and signed
a consent form to participate in a research protocol. In
the majority of cases, individuals in this database have participated
in more than one protocol. This is quite unlike a practice database of
patients as the people in our research database have already self-selected
themselves as being interested in participating in research protocols,
whereas only 1-3% of a patient database is likely to volunteer for a research
study. A summary of the some of the key characteristics of individuals
in this protocol follow:
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