| Literature DB >> 7954280 |
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.Entities:
Mesh:
Year: 1994 PMID: 7954280 DOI: 10.1002/1097-0142(19941101)74:9+<2647::aid-cncr2820741811>3.0.co;2-x
Source DB: PubMed Journal: Cancer ISSN: 0008-543X Impact factor: 6.860