Daubert v. Merrell Dow Pharmaceuticals, Inc.
Facts
Petitioners were children born with serious birth defects whose parents alleged the defects were caused by the mothers' ingestion of Bendectin during pregnancy. Merrell Dow moved for summary judgment and supported the motion with an expert affidavit stating that review of more than 30 published studies involving over 130,000 patients showed no study finding Bendectin to be a human teratogen. Petitioners did not dispute that characterization of the published epidemiological record, but offered eight experts who concluded Bendectin could cause birth defects based on animal studies, chemical-structure analyses, and reanalysis of previously published epidemiological studies. The lower courts excluded that evidence largely because it was not generally accepted, and in part because the reanalyses had not been published or peer reviewed.
Issue
Does the Frye general-acceptance test govern the admissibility of expert scientific testimony in federal trials after adoption of the Federal Rules of Evidence? If not, what standard must federal trial judges apply under the Rules when deciding whether to admit scientific expert testimony?
Rule
Frye's general-acceptance test does not control the admissibility of expert scientific testimony in federal court because it was superseded by the Federal Rules of Evidence. Under Rule 702, the trial judge must act as a gatekeeper and ensure that proffered scientific expert testimony is both relevant and reliable: it must constitute scientific knowledge grounded in the methods and procedures of science and must assist the trier of fact by fitting the facts in issue. In making that preliminary Rule 104(a) determination, the court may consider factors such as whether the theory or technique can be and has been tested, whether it has been subjected to peer review and publication, its known or potential error rate, the existence of standards controlling its operation, and its degree of general acceptance.
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