Plаintiffs Jason Daubert and Eric Schul-ler suffer from limb reduction birth defects. They allege that these defects resulted from the fact that their mothers used Bendectin, a prescription anti-nausea drug, during pregnancy. The plaintiffs seek damages from the drug’s manufacturer, defendant Merrell Dow Pharmacеuticals.
Plaintiffs’ evidence of causation consisted primarily of expert opinion based on in vitro and in vivo animal tests, chemical structure analyses and the reanalysis of epidemiological studies. Among the contrary evidence proffered by Merrell Dow was the affidavit of a physiciаn and epidemiologist who reviewed all of the available literature on the subject, which included more than 30 published studies involving over 130,000 patients, and concluded that no published epidemiological study had demonstrated a statistically significant association between Bendectin and birth defects. Plaintiffs do not challenge this summary of the published record.
The district court determined that plaintiffs could not meet their burden of proving thаt Bendectin caused Jason’s and Eric’s birth defects and granted Merrell Dow’s motion for summary judgment. Daubert v. Merrell Dow Pharmaceuticals, Inc.,
A. Expert opinion based on a scientific techniquе “is admissible if it is generally accepted as a reliable technique among the scientific community.” United States v. Solomon,
For expert opinion based on a given scientific methodology to bе admissible, the methodology cannot diverge significantly from the procedures accepted by recognized authorities in the field. If it does sо diverge, it cannot be shown to be “generally accepted as a reliable technique,” Solomon,
B. Whether Bendectin is responsible for limb reduction defects is not a new question in the federal courts. Four of our sister circuits have considered whether plaintiffs could establish such responsibility in the absence of critically analyzed epidemiological studies establishing a connection between the use of the drug and the birth defects. DeLuca v. Merrell Dow Pharmaceuticals, Inc.,
Plaintiffs argue that reanalysis is a generally accepted scientific technique, so it follows that their experts were basing
C. Lynch, Richardson and Brock reflect a well-founded skepticism of the scientific value of the reanalysis methodology employed by plaintiffs’ experts; they recognize that “[t]he best test of certаinty we have is good science — the science of publication, replication, and verification, the science of consensus аnd peer review.” P. Huber, Galileo’s Revenge: Junk Science in the Courtroom 228 (1991). For the convincing reasons articulated by our sister circuits, we agree with the district court that the available animal and chemical studies, together with plaintiffs’ expert reanalysis of epidemiological studies, provide insufficient foundation to allow admission of expert testimony to the effect that Bendectin caused plaintiffs’ injuries. Accordingly, plaintiffs could not satisfy their burden of proving causation аt trial. See Christophersen,
AFFIRMED.
Notes
. Richardson and Lynch held that expert testimony that Bendectin caused birth defects, based solely on аnimal and chemical tests and reana-lyses of epidemiological studies, was inadmissible under Federal Rule of Evidence 703, and therefore thаt plaintiffs had failed to present evidence to support a jury verdict in their favor.
. The Third Circuit has left open the possibility that expert testimony based on the reanalysis of epidеmiological studies may be admissible if it
. Scientific studies conducted in anticipation of litigation must be scrutinized muсh more carefully than studies conducted in the normal course of scientific inquiry. This added dose of skepticism is warranted, in part, because studiеs generated especially for use in litigation are less likely to have been exposed to the normal peer review process, which is one of the hallmarks of reliable scientific investigation. See Brock,
