City of Huntington, West Virginia v. AmerisourceBergen Drug Corporation

CourtDistrict Court, S.D. West Virginia
DecidedFebruary 15, 2022
Docket3:17-cv-01362
StatusUnknown

This text of City of Huntington, West Virginia v. AmerisourceBergen Drug Corporation (City of Huntington, West Virginia v. AmerisourceBergen Drug Corporation) is published on Counsel Stack Legal Research, covering District Court, S.D. West Virginia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
City of Huntington, West Virginia v. AmerisourceBergen Drug Corporation, (S.D.W. Va. 2022).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE SOUTHERN DISTRICT OF WEST VIRGINIA THE CITY OF HUNTINGTON, Plaintiff, v. CIVIL ACTION NO. 3:17-01362 AMERISOURCEBERGEN DRUG CORPORATION, et al., Defendants. ________________________________ CABELL COUNTY COMMISSION, Plaintiff, v. CIVIL ACTION NO. 3:17-01665 AMERISOURCEBERGEN DRUG CORPORATION, et al., Defendants. ________________________________ MEMORANDUM OPINION AND ORDER Pending before the court is defendants’ motion to exclude certain Rule 30(b)(6) testimony of Thomas Prevoznik. See ECF No. 1310. That motion is fully briefed and, for the reasons discussed herein, it is DENIED. I. These two cases, arising out of the opioid epidemic, are related to thousands of other lawsuits that have been filed throughout the country since 2017. “These cases concern the alleged improper marketing of and inappropriate distribution of various prescription opiate medications into cities, states, and towns across the country.” In re Nat'l Prescription Opiate Litig., 290 F. Supp.3d 1375, 1377 (J.P.M.L. 2017). The Opioid MDL (MDL 2804) was created by the Judicial Panel on Multidistrict Litigation (JPML) in December of 2017 after the JPML determined that a large number of cases should be centralized for pretrial proceedings in the Northern District of Ohio to coordinate the resolution of these actions. See id. at 1378. Since MDL 2804's formation, well over 2,000 cases have been transferred to the MDL court. See In re Nat'l Prescription Opiate Litig., No. 1:17-MD-2804, 2019 WL 4686815, at *1 (N.D. Ohio Sept. 26, 2019). In his management of the MDL, Judge Dan Polster, the presiding judge, has overseen “discovery involving over 450 depositions and over 160 million pages of documents” and ruled “on innumerable discovery motions, ranging from the trivial to motions to compel production of documents from the United States Drug Enforcement Agency”. Id. at *2. Specifically, with respect to the DEA, Judge Polster notes that “the DEA and the parties thoroughly and vigorously negotiated the scope of MDL discovery, in light of the needs of the case and the burden on

the DEA as a non-party, governmental agency. Disputes were mediated and resolved by Special Master Cohen. Ultimately, DEA produced thousands of pages of documents and provided several witnesses for lengthy deposition.” ECF No. 502-1. 2 In response to defendants’ subpoenae, one of the witnesses DEA tapped to testify in the MDL was Thomas Prevoznik. At the time of his deposition in April 2019, Prevoznik was a 28-year veteran of the DEA. See ECF No. 1355-7. Hired as a Diversion Investigator in 1991, Prevoznik moved up the ranks at DEA and, as of his deposition, was the Associate Section Chief for the DEA’s Diversion Control Division in the Pharmaceutical Investigations Section. See id. Not only did Prevoznik hold a number of different positions over the course of his DEA career, he also served the agency in several different geographic areas before moving to DEA headquarters in May 2012 to become a Diversion Staff Coordinator. See id. The particulars of Prevoznik’s deposition (as well as the other DEA witnesses) were negotiated between the parties and the DEA and overseen by Special Master Cohen. See, e.g., ECF No. 1355-4. In response to plaintiffs’ and defendants’ requests and subject to certain limitations, the DOJ authorized Prevoznik to testify as to the following topics: Def. Topic 2: Your interpretation and enforcement of, and practices related to 21 U.S.C. § 823 and 21 C.F.R. § 1301.74. • DEA’s policies, practices, and guidance relating to whether registrants are permitted to ship orders of controlled substances that the registrant determines to be “suspicious” and/or “excessive,” including the nature of the purported duty to conduct due diligence on such orders, as described in the 2006 and 2007 letters from DEA to 3 registrants, and any changes to those policies, practices, and guidance over time; • DEA’s interpretation of, and policies and practices relating to, what constitutes a “suspicious order” under 21 C.F.R. § 1301.74(b), and any changes thereto over time; • DEA’s interpretation of, and policies and practices relating to, registrants’ obligations to “know their customers” and/or “know their customers’ customers,” and any changes thereto over time; • DEA’s guidance and/or directions given to registrants about suspicious order reports, including the scope, format, types of systems to be utilized (including automated systems), and DEA locations (field offices or headquarters) for such submissions, and how such guidance changed over time. Def. Topic 3: Guidance or other Communications provided by You to Defendants, whether written or oral, regarding the criteria for what makes an order for controlled substances “suspicious” under 21 C.F.R. § 1301.74. • DEA’s guidance to registrants relating to whether registrants are permitted to ship orders of controlled substances that the registrant determines to be “suspicious” and/or “excessive,” including the nature of the purported duty to conduct due diligence, as described in the 2006 and 2007 letters from DEA to registrants, and any changes in that guidance over time; • DEA’s guidance to registrants relating to what constitutes a “suspicious order” under 21 C.F.R. § 1301.74(b), and any changes in that guidance over time; • DEA’s “Distributor Briefing” initiative, including when these briefings were given and the guidance provided to registrants relating to their obligations under the CSA; 4 • DEA’s guidance to registrants relating to the adequacy of their suspicious order monitoring systems; and • DEA’s guidance to registrants relating to any obligation to monitor registrants’ customers and the downstream supply chain. Def. Topic 9: Your procedures and practices relating to obtaining, processing, analyzing, and taking formal or informal actions based upon the ARCOS Data, Suspicious Order Reports, or other Communications from DEA Registrants to identify and stop sources of diversion. This topic encompasses the following subjects: • DEA’s general procedures relating to the analysis of ARCOS data, Suspicious Order Reports, or other Communications from DEA Registrants identifying suspicious orders or customers from 1995 to 2014, but not including DEA’s analysis of particular ARCOS data or Suspicious Order Reports. Def. Topic 12: Your decision not to allow DEA- registered distributors access to de-identified ARCOS Data prior to February 2018, and your decisions to provide DEA-registered distributors with limited access to certain ARCOS Data in February. Pl. Topic 1: DEA’s interpretation of the Comprehensive Drug Abuse Prevention and Control Act of 1970, 21 U.S.C. § 801 et seq. (“CSA” or “Controlled Substances Act”) and its implementing regulations, including but not limited to, 21 C.F.R. § Part 1300 et seq. (including, but not limited to, 21 C.F.R. §§ 1301.11, 1301.74), 21 C.F.R. Part 1305, and 28 C.F.R. § 0.100 with respect to a registrant’s obligation “to main[tain] . . .

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Los Angeles Times Communications, LLC v. Department of the Army
442 F. Supp. 2d 880 (C.D. California, 2006)
United States v. Christie
624 F.3d 558 (Third Circuit, 2010)
Industrial Hard Chrome, Ltd. v. Hetran, Inc.
92 F. Supp. 2d 786 (N.D. Illinois, 2000)
PPM Finance, Inc. v. Norandal USA, Inc.
392 F.3d 889 (Seventh Circuit, 2004)
Va. Dep't of Corr. v. Jordan
921 F.3d 180 (Fourth Circuit, 2019)
Sara Lee Corp. v. Kraft Foods Inc.
276 F.R.D. 500 (N.D. Illinois, 2011)

Cite This Page — Counsel Stack

Bluebook (online)
City of Huntington, West Virginia v. AmerisourceBergen Drug Corporation, Counsel Stack Legal Research, https://law.counselstack.com/opinion/city-of-huntington-west-virginia-v-amerisourcebergen-drug-corporation-wvsd-2022.