THIS DOCUMENT RELATES TO C. R. BARD WAVE 4 & WAVE 5 CASES BEFORE JUDGE GOODWIN:
JOSEPH R. GOODWIN, District Judge.
Pending in In re C. R. Bard, Inc., 2:10-md-2187, MDL 2187, is defendant C. R. Bard, Inc. ("Bard")'s Daubert Motion to Exclude the Opinions and Testimony of Alan Garely, M.D. [ECF No. 4561]. The motion is now ripe for consideration because the briefing is complete. As set forth below, Bard's motion is
This case resides in one of seven MDLs assigned to me by the Judicial Panel on Multidistrict Litigation concerning the use of transvaginal surgical mesh to treat pelvic organ prolapse ("POP") and stress urinary incontinence ("SUI"). In the seven MDLs, there are more than 16,000 cases currently pending, approximately 1,500 of which are in the Bard MDL, 2187 MDL.
In this MDL, the court's tasks include "resolv[ing] pretrial issues in a timely and expeditious manner" and "resolv[ing] important evidentiary disputes." Barbara J. Rothstein & Catherine R. Borden, Fed. Judicial Ctr., Managing Multidistrict Litigation in Products Liability Cases 3 (2011). In an effort to manage the massive Bard MDL efficiently and effectively, the court decided to conduct pretrial discovery and motions practice on an individualized basis. To this end, I selected certain cases to become part of a "wave" of cases to be prepared for trial and, if necessary, remanded.
Upon the creation of a wave, a docket control order subjects each case in the wave to the same scheduling deadlines, rules regarding motion practice, and limitations on discovery. See, e.g., Pretrial Order ("PTO") # 236 (establishing Wave 4); PTO # 244 (establishing Wave 5). To handle motions to exclude or to limit expert testimony pursuant to Daubert v. Merrell Dow Pharmaceuticals, Inc., 509 U.S. 579 (1993), the court developed a specific procedure for cases designated in Wave 4 and Wave 5. The court instructed the parties to file briefing on general causation issues in the main MDL, MDL 2187, while specific causation Daubert motions, responses, and replies were to be filed in the individual member cases. To the extent that an expert is both a general and specific causation expert, the court advised the parties that they could file a general causation motion in the main MDL and a specific causation motion in an individual member case. See PTO # 236, at 4; PTO # 244, at 4.
Under Federal Rule of Evidence 702, expert testimony is admissible if it will "help the trier of fact to understand the evidence or to determine a fact in issue" and (1) is "based upon sufficient facts or data" and (2) is "the product of reliable principles and methods" which (3) has been reliably applied "to the facts of the case." Fed. R. Evid. 702. A two-part test governs the admissibility of expert testimony. The evidence is admitted if it "rests on a reliable foundation and is relevant." Daubert v. Merrell Dow Pharm., 509 U.S. 579, 597 (1993). The proponent of expert testimony does not have the burden to "prove" anything. However, he or she must "come forward with evidence from which the court can determine that the proffered testimony is properly admissible." Md. Cas. Co. v. Therm-O-Disc, Inc., 137 F.3d 780, 783 (4th Cir. 1998).
The district court is the gatekeeper. It is an important role: "[E]xpert witnesses have the potential to be both powerful and quite misleading"; the court must "ensure that any and all scientific testimony . . . is not only relevant, but reliable." Cooper v. Smith & Nephew, Inc., 259 F.3d 194, 199 (4th Cir. 2001) (citing Daubert, 509 U.S. at 588, 595; Westberry v. Gislaved Gummi AB, 178 F.3d 257, 261 (4th Cir. 1999)). I "need not determine that the proffered expert testimony is irrefutable or certainly correct" — "[a]s with all other admissible evidence, expert testimony is subject to testing by `[v]igorous cross-examination, presentation of contrary evidence, and careful instruction on the burden of proof.'" United States v. Moreland, 437 F.3d 424, 431 (4th Cir. 2006) (alteration in original) (quoting Daubert, 509 U.S. at 596); see also Md. Cas. Co., 137 F.3d at 783 ("All Daubert demands is that the trial judge make a `preliminary assessment' of whether the proffered testimony is both reliable . . . and helpful.").
Daubert mentions specific factors to guide the overall relevance and reliability determinations that apply to all expert evidence. They include (1) whether the particular scientific theory "can be (and has been) tested"; (2) whether the theory "has been subjected to peer review and publication"; (3) the "known or potential rate of error"; (4) the "existence and maintenance of standards controlling the technique's operation"; and (5) whether the technique has achieved "general acceptance" in the relevant scientific or expert community. United States v. Crisp, 324 F.3d 261, 266 (4th Cir. 2003) (quoting Daubert, 509 U.S. at 593-94).
Despite these factors, "[t]he inquiry to be undertaken by the district court is `a flexible one' focusing on the `principles and methodology' employed by the expert, not on the conclusions reached." Westberry, 178 F.3d at 261 (quoting Daubert, 509 U.S. at 594-95); see also Kumho Tire Co. v. Carmichael, 526 U.S. 137, 150 (1999) ("We agree with the Solicitor General that `[t]he factors identified in Daubert may or may not be pertinent in assessing reliability, depending on the nature of the issue, the expert's particular expertise, and the subject of his testimony.'" (citation omitted)); see also Crisp, 324 F.3d at 266 (noting "that testing of reliability should be flexible and that Daubert's five factors neither necessarily nor exclusively apply to every expert").
With respect to relevancy, Daubert also explains:
Daubert, 509 U.S. at 591-92 (citations and internal quotation marks omitted).
Dr. Alan Garely is board-certified in obstetrics, gynecology, female pelvic medicine and reconstructive surgery. See Pls.' Resp. in Opp'n to Def.'s Mot. to Exclude Certain Ops. of Alan Garely, M.D., at 1 [ECF No. 4599]. He offers several different opinions, a number of which Bard contends are improper: (1) narrative descriptions of Bard documents that purport to address Bard's knowledge, state of mind, or corporate conduct; (2) legal opinions; and (3) opinions about the adequacy of the warnings contained in the Instructions for Use ("IFU").
A portion of Dr. Garely's expert report discusses Bard's knowledge and state of mind. Dr. Garely opines, for example, that:
Defs.' Motion to Exclude the Ops. & Test. of Alan Garely, M.D., Ex. 1 ("Dr. Garely's Expert Report") at 14-15 [ECF No. 4561-2].
While an expert may testify as to a review of internal corporate documents solely for the purpose of explaining the basis for his or her opinions—assuming the opinions are otherwise admissible—Bard's knowledge, state of mind, or other matters related to corporate conduct are not appropriate subjects of expert testimony because opinions on these matters will not assist the jury. See, e.g., In re Fosamax Prods. Liab. Litig., 645 F.Supp.2d 164, 192 (S.D.N.Y. 2009) (precluding testimony as to "the knowledge, motivations, intent, state of mind, or purposes of" a company and its employees because it "is not a proper subject for expert or even lay testimony"). Accordingly, Bard's motion is
In the Fourth Circuit, "opinion testimony that states a legal standard or draws a legal conclusion by applying law to the facts is generally inadmissible." United States v. McIver, 470 F.3d 550, 562 (4th Cir. 2006). Bard seeks to exclude certain opinions expressed by Dr. Garely that it believes amount to legal conclusions. For instance, Bard argues that Dr. Garely should be prevented from testifying that "omission of instructions or warnings . . . rendered the Align TO device not reasonably safe" and that the design of the Align TO was "unreasonably dangerous and defective" because they state a legal standard or draw a legal conclusion. See Def. Mem. of Law in Supp. of Mot. to Exclude Certain Ops. of Alan Garely, M.D., at 7 (citing Dr. Garely's Expert Report, at 6, 13). The plaintiffs, in response, do not believe that these statements draw legal conclusions from the facts. I disagree.
Here, Dr. Garely's opinion goes a step beyond the adequacy of the warnings or the efficacy of the product's design. In doing so, these opinions invade the province of the jury by stating a legal conclusion and will not be accepted at trial. See United States v. McIver, 470 F.3d 550, 562 (4th Cir. 2006) ("[O]pinion testimony that states a legal standard or draws a legal conclusion by applying law to the facts is generally inadmissible."); see also Perez v. Townsend Eng'g Co., 562 F.Supp.2d 647, 652 (M.D. Pa. 2008) (precluding an expert witness "from using legal terms of art" and "giv[ing] legal conclusions, such as, but not limited to, the conclusions that the [product] was `defective,' `unreasonably dangerous,' or was the `proximate cause' of [the plaintiff's] injury"). Therefore, Bard's motion on this point is
Previously, in September 2016, I held that Dr. Garely is not qualified to opine on the adequacy of a product warning IFU merely because it included risks he has observed in his own practice without additional expertise in the specific area of product warnings. See In re: Ethicon Inc. Pelvic Repair Sys. Prod. Liab. Litig., MDL No. 2327, 2016 WL 4582209, at *3 (S.D. W. Va. Sept. 1, 2016) ("Dr. Garely does not possess the additional expertise to offer expert testimony about what an IFU should or should not include.").
According to Bard, Dr. Garely remains unqualified to offer expert testimony on the adequacy of the Align product's IFU because he has no specialized knowledge of IFUs beyond his experience as a physician.
In response, in order to justify deviation from this court's prior reasoning, the plaintiffs cite Dr. Garely's deposition testimony wherein he details his involvement in the development of the IFU for the TVT sling device. See Pls.' Resp. in Opp'n to Def.'s Mot. to Exclude Certain Ops. of Alan Garely, M.D., at 14 [ECF No. 4599] (citing Ex. 2 ("Dr. Garely Dep.") 42:6-45:11 [ECF No. 4561-3]). Specifically, Dr. Garely stated:
Id. (emphasis added).
While this testimony further elucidates Dr. Garely's qualifications to testify about the risks of implanting a product and whether those risks were adequately expressed on the product's IFU, see In re Yasmin & Yaz (Drospirenone) Prods. Liab. Litig., 2011 WL 6301625, at *11 (S.D. Ill. Dec. 16, 2011) ("[D]octors are fully qualified to opine on the medical facts and science regarding the risks and benefits of drugs and to compare that knowledge with what was provided in the text of labeling and warnings. . . ." (internal quotations and brackets omitted)), Dr. Garely remains unqualified to opine on whether an IFU complies with regulatory standards because his "additional expertise" — identified above — in the area of product warning derives from his general experience as a physician. See Dr. Garely Dep. 56:7-8 ("I'm not an expert on industry regulations."). Accordingly, Bard's motion on this point is
To summarize, I
The court