Anderson v. Department Of Health And Human Services

907 F.2d 936, 1990 U.S. App. LEXIS 10113
CourtCourt of Appeals for the Tenth Circuit
DecidedJune 22, 1990
Docket86-2246
StatusPublished
Cited by41 cases

This text of 907 F.2d 936 (Anderson v. Department Of Health And Human Services) is published on Counsel Stack Legal Research, covering Court of Appeals for the Tenth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Anderson v. Department Of Health And Human Services, 907 F.2d 936, 1990 U.S. App. LEXIS 10113 (10th Cir. 1990).

Opinion

907 F.2d 936

Celia ANDERSON, Plaintiff-Appellant,
v.
DEPARTMENT OF HEALTH AND HUMAN SERVICES; Margaret Heckler,
Secretary, Department of Health and Human Services; Food
and Drug Administration; and Dr. Frank Young, M.D.,
Commissioner, Food and Drug Administration, Defendants-Appellees,
and
Dow Corning Corporation, Defendant/Intervenor-Appellee.

Nos. 86-2246, 86-2495.

United States Court of Appeals,
Tenth Circuit.

June 22, 1990.

Daniel F. Bertch of Robert J. Debry & Associates (Robert J. Debry of Robert J. Debry & Associates, with him on the brief), Salt Lake City, Utah, for plaintiff-appellant.

Burt A. Braverman of Cole, Raywid & Braverman, Washington, D.C. (Susan Paradise Baxter and Kenneth A. Grant of Cole, Raywid & Braverman, Washington, D.C., Ray R. Christensen of Christensen, Jensen & Powell, Salt Lake City, Utah, and Harvey Steinberg of Dow Corning Corp., Midland, Mich., with him on the brief), for defendant/intervenor-appellee.

Before HOLLOWAY, Chief Judge, and BARRETT and EBEL, Circuit Judges.

EBEL, Circuit Judge.

This appeal concerns plaintiff-appellant Celia Anderson's attempt under the Freedom of Information Act ("FOIA"), 5 U.S.C. Sec. 552, to compel defendant-appellee Food and Drug Administration ("FDA") to disclose certain documents submitted to the FDA by defendant-intervenor Dow Corning Corporation. The district court granted summary judgment to defendants, holding that the requested documents contain confidential information that is exempt from the disclosure requirements of the FOIA. We affirm in part, reverse in part, and remand.

The following issues are raised on appeal: (1) whether Exemption 4 of the FOIA, 5 U.S.C. Sec. 552(b)(4), allowed the FDA to refuse to disclose all of the documents at issue; (2) whether 18 U.S.C. Sec. 1905, 21 U.S.C. Sec. 360j(c), or 21 U.S.C. Sec. 331(j) justify nondisclosure of the documents pursuant to Exemption 3 of the FOIA, 5 U.S.C. Sec. 552(b)(3); and (3) whether the district court should have vacated its judgment pursuant to Federal Rule of Civil Procedure 60(b)(3).

FACTS

Appellant sued Dow in state court for injuries allegedly caused by an injection of liquid silicone manufactured by Dow.1 In connection with her state suit, appellant submitted a FOIA request to the FDA in order to obtain over 16,000 pages of documents that Dow had submitted to the FDA concerning Dow's liquid silicone, which is still in the testing phase and for which Dow has been seeking FDA approval for over 20 years. The FDA rejected appellant's request.

The documents at issue consist of over 16,000 pages contained in a Notice of Claimed Investigational Exemption for a New Drug ("IND"), a New Drug Application ("NDA"), and an Application for an Investigational Device Exemption ("IDE"), all submitted by Dow to the FDA. An IND is filed as a precondition to clinical testing of a drug. 21 U.S.C. Sec. 355(i), 21 C.F.R. Sec. 312.50. Once the IND is approved by the FDA, the sponsor of the new drug can ship the drug for use in clinical tests, the results of which are reported to the FDA. 21 C.F.R. Sec. 312.10. When adequate evidence of complete clinical testing has been submitted to the FDA, the sponsor may file an NDA, the approval of which is required before a drug can be marketed in interstate commerce. 21 U.S.C. Sec. 355(a), (b), and (j). The NDA must contain extensive data regarding the composition, manufacture, and effects of the drug, including full reports of clinical and nonclinical investigations, adverse reaction reports, and published articles on the effectiveness of the drug. 21 C.F.R. Sec. 314.50.

After Dow filed its IND for injectable silicone, amendments to the Food, Drug, and Cosmetic Act were passed, giving the FDA regulatory authority over medical devices. As a result of those amendments, injectable silicone was reclassified from a drug to a medical device, and Dow was required to convert its IND to an Application for an Investigational Device Exemption ("IDE"), the medical device equivalent of an IND. See 21 U.S.C. Sec. 360j(g); 21 C.F.R. Sec. 812.20. Dow's IDE essentially contains the research that has been carried out by Dow under its IND and NDA.2

Appellant brought suit in the district court seeking disclosure of the documents in the IND, NDA and IDE pursuant to the FOIA. Dow intervened and has defended the action on behalf of the FDA. Dow prepared an eighty-five page "Vaughn index"3 listing roughly 16,000 documents at issue by in-house number. Across from the entries was a brief description of the document(s) and a coded explanation referring to one of seven specific categories of information "for which confidentiality is claimed:"

1. Manufacturing and processing information, including formulations, chemistry and quality assurance procedures.

2. Protocols, including forms for reporting results of research and informational materials supplied to clinical investigators.

3. Preclinical test data.

4. Clinical test data including adverse reaction reports and interim data.

5. Patient information.

6. Contractor and consultant identities.

7. Marketing, sales and customer information.

Vaughn Index at iv. In addition to those brief explanations, Dow filed as an exhibit the affidavit of Robert T. Rylee, II, a Vice President and General Manager of Dow. In that affidavit, Mr. Rylee provided more thorough explanations of the seven justifications listed in the Vaughn index. However, Mr. Rylee's affidavit did not elaborate on the description or asserted justification for nondisclosure of the individual documents.

For approximately half of the documents listed in the Vaughn index, no coded explanation entry appeared. Instead, Dow had written "n/a" in the explanation column. In the introduction to the Vaughn index, Dow explained its reasons for not disclosing those documents for which no explanation had been offered:

This index identifies portions of the documents at issue that are subject to withholding because they contain privileged or confidential commercial information or trade secrets within the meaning of Exemption 4 of the Freedom of Information Act, 5 U.S.C. Sec. 552, and the Trade Secrets Act, 18 U.S.C. Sec. 1905. However, Dow Corning also asserts that all of the documents at issue, including documents or portions of documents that have not been identified in this index as falling within Exemption 4 or the Trade Secrets Act, are required to be withheld pursuant to Defendant FDA's statutory authority and implementing regulations.

Vaughn Index at iv-v.4

The district court granted Dow's motion for summary judgment, determining that there were no material facts in dispute and holding that the documents at issue are exempt from disclosure pursuant to Exemptions 3 and 4 of the FOIA, 5 U.S.C. Sec. 552(b)(3) & (4), and are prohibited from disclosure under 18 U.S.C.

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Cite This Page — Counsel Stack

Bluebook (online)
907 F.2d 936, 1990 U.S. App. LEXIS 10113, Counsel Stack Legal Research, https://law.counselstack.com/opinion/anderson-v-department-of-health-and-human-services-ca10-1990.