Abstract:
:Quality assurance for the management of multicenter clinical trials requires timely patient and data accrual and consistency with design parameters. Data from central pathology review, treatment modality, and follow-up as well as trial end points direct the selection of appropriate compliance measures. To integrate these data to monitor group performance on a specific protocol, to monitor discipline performance, or to monitor an institution's performance is a formidable task. This is especially true for a group such as the Pediatric Oncology Group, where there are a large number of protocols, many diseases, and widely differing protocol requirements. Quality assurance methods for the Pediatric Oncology Group are discussed.
journal_name
Cancerjournal_title
Cancerauthors
Pollock BHdoi
10.1002/1097-0142(19941101)74:9+<2647::aid-cncr282subject
Has Abstractpub_date
1994-11-01 00:00:00pages
2647-52issue
9 Suppleissn
0008-543Xissn
1097-0142journal_volume
74pub_type
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