Daubert v Merrell Dow Pharmaceuticals, Inc. (1993): Case Summary and Legal Principles

Court: U.S. Supreme Court
Judgment Date: 28 June 1993
Where Reported: 509 U.S. 579 (1993)

Legal Issues in Daubert v Merrell Dow Pharmaceuticals, Inc.

Daubert v Merrell Dow Pharmaceuticals, Inc. centred on the admissibility of expert scientific testimony in federal trials.

The legal issue at hand was whether the “general acceptance” standard established in Frye v United States was still applicable under the Federal Rules of Evidence.

Daubert v Merrell Dow Pharmaceuticals questioned how federal courts should determine whether scientific evidence is sufficiently reliable and relevant to be presented to a jury.

The core issue was how to assess the scientific validity of expert testimony, especially when based on emerging or non-traditional scientific methods and theories, and its appropriateness in a legal setting.

Material Facts in Daubert v Merrell Dow Pharmaceuticals, Inc.

In Daubert, the petitioners, two families whose children were born with birth defects, sued Merrell Dow Pharmaceuticals alleging that the defects were caused by the mothers’ ingestion of Bendectin, a drug manufactured by Merrell Dow.

Daubert v Merrell Dow Pharmaceuticals, Inc. - federal rule of evidence - expert testimony

The plaintiffs offered expert testimony based on animal studies, pharmacological comparisons, and reanalyses of previously published human epidemiological studies to support their claim.

The District Court granted summary judgment for Merrell Dow, ruling the expert evidence inadmissible under the “general acceptance” standard from Frye v United States.

This standard required that for scientific evidence to be admissible, it must be generally accepted in the relevant scientific community.

The Ninth Circuit Court of Appeals affirmed the decision, leading to the Supreme Court review.

Judgment v Daubert v Merrell Dow Pharmaceuticals, Inc.

The Supreme Court vacated the judgment of the Ninth Circuit and remanded the case, holding that the Federal Rules of Evidence, and not the Frye standard, governed the admissibility of expert scientific testimony.

The Court established that under the Federal Rules of Evidence, particularly Rule 702, the trial judge must ensure that any scientific testimony is not only relevant but also reliable.

The ruling shifted the focus from the “general acceptance” of the scientific method or principle to the scientific validity and relevance of the methodology underlying the expert’s testimony.

The Reason for the Decision in Daubert v Merrell Dow Pharmaceuticals, Inc.

The Supreme Court’s decision was rooted in an interpretation of the Federal Rules of Evidence as providing a more flexible and comprehensive framework for evaluating scientific evidence than the Frye standard.

The Court emphasised that the determination of scientific validity should not be solely based on general acceptance within the scientific community.

Instead, the Court suggested a multifactorial approach, considering factors such as whether the theory or technique can be tested, whether it has been subject to peer review and publication, its known or potential error rate, and the existence and maintenance of standards controlling its operation.

The Court recognised that scientific knowledge evolves and that restricting evidence to only generally accepted theories could hinder the legal process’s access to valuable scientific insights.

This approach allowed for a broader range of scientific methods and theories, including those that are new or unconventional, to be considered in legal proceedings.

The focus shifted to the judge’s role as a gatekeeper in assessing the relevance and reliability of the scientific evidence, rather than relying on the scientific community’s consensus.

The decision also emphasised that scientific validity and relevance are separate inquiries.

The validity inquiry focuses on whether the expert’s testimony is based on a scientifically valid principle or method, while the relevance inquiry looks at whether the testimony is applicable to the facts of the case.

The decision in Daubert v Merrell Dow Pharmaceuticals thus underscored the importance of the trial judge’s preliminary assessment of the scientific basis of the expert’s testimony, ensuring it is not only pertinent to the case but also grounded in a methodologically sound scientific process.

Legal Principles in Daubert v Merrell Dow Pharmaceuticals, Inc.

Daubert v Merrell Dow Pharmaceuticals, Inc. established key legal principles regarding the admissibility of scientific evidence in federal courts.

It affirmed that under the Federal Rules of Evidence, specifically Rule 702, the trial judge has the responsibility to ensure that expert testimony is both reliable and relevant.

The decision moved away from the Frye standard’s “general acceptance” test to a more flexible approach that considers various factors in determining scientific validity.

This case set a precedent for a more nuanced evaluation of evidence in court, emphasising the role of the judge in scrutinising the basis of scientific testimony, rather than deferring to the consensus within the scientific community.

This approach allows for the inclusion of innovative and emerging scientific theories in legal proceedings, broadening the scope of admissible scientific evidence.

Picture of Ben Shaw-Parker, Ph.D.

Ben Shaw-Parker, Ph.D.

Ben is a university law professor. He has an LLM in Public International Law and a Doctorate in Humanitarian Law. Ben's specialty is in the area of Human Rights, Crime Law, Socio-legal Studies, Common Law, Comparative Law, Public Law and Environmental Law. He has contributed to several law journals.

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