What people are saying - Write a review
We haven't found any reviews in the usual places.
QUANTITATIVE CHARACTERIZATION OF CLINICAL TRIALS
CONTEXTS FOR CLINICAL TRIALS
4 other sections not shown
administrative agent analysis and reporting chapter Clinical Trials Completed Completed in FY computer files computer software computer systems concurrent control conduct stage control group cost data and safety data collection forms data forms data management Design Parameters determine develop documents duration EKGs eligibility endpoints error evaluate executive committee funding GCRC information processing functions informed consent Initiation/Organization Stage institute staff institutes except NCI institutional review board inventory manual of operations methods multicenter clinical trial multicenter trial National Eye Institute NHLBI NIAID NICHD NINCDS number of subjects number of trials participating centers patients percent performed pharmaceutical phase physicians planning stage potential principal investigator problems procedures protocol and manual randomization reading center recruiting Reporting Stage responsible safety monitoring committee sample size single-center trial special centers Sponsoring Institute statistical statistician steering committee stopping rules tion treatment group treatments to subjects trial governance group