Dr. Charles W. McCutchen Appellee/cross-Appellant v. U.S. Department of Health and Human Services, Appellant/cross-Appellee

30 F.3d 183, 308 U.S. App. D.C. 121, 1994 U.S. App. LEXIS 20250
CourtCourt of Appeals for the D.C. Circuit
DecidedAugust 5, 1994
Docket92-5372 & 92-5389
StatusPublished
Cited by59 cases

This text of 30 F.3d 183 (Dr. Charles W. McCutchen Appellee/cross-Appellant v. U.S. Department of Health and Human Services, Appellant/cross-Appellee) is published on Counsel Stack Legal Research, covering Court of Appeals for the D.C. Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Dr. Charles W. McCutchen Appellee/cross-Appellant v. U.S. Department of Health and Human Services, Appellant/cross-Appellee, 30 F.3d 183, 308 U.S. App. D.C. 121, 1994 U.S. App. LEXIS 20250 (D.C. Cir. 1994).

Opinion

Opinion for the court filed by Circuit Judge BUCKLEY.

BUCKLEY, Circuit Judge:

Dr. Charles McCutchen filed a request under the Freedom of Information Act for a list of all investigations of scientific misconduct undertaken by the Department of Health and Human Services’ Office of Scientific Integrity. The Department released this list, but in all cases where there had been no finding of wrongdoing, it deleted the names of both the investigated scientists (“respondents”) and the individuals who had made the allegations of misconduct (“complainants”). After Dr. McCutchen sued to compel disclosure of these names, the district court ordered the Department to disclose those of the respondents but permitted it to withhold those of the complainants. The Department appeals and Dr. McCutchen cross-appeals from this order. Because we find that the privacy interests of both the respondents and the complainants outweigh the public interest in disclosure, we reverse the ruling requiring disclosure of the respondents’ names and affirm the ruling approving the withholding of the complainants’ names.

I. BACKGROUND'

A. Freedom of Information Act We recently observed that “[t]he purpose of the Freedom of Information Act, 5 U.S.C. § 552 (1988) (“FOIA”), is to facilitate public access to Government documents” and that “[FOIA] is meant to pierce the veil of administrative secrecy and to open agency action to the light of public scrutiny.” Beck v. Dep’t of Justice, 997 F.2d 1489, 1490 (D.C.Cir.1993) (internal quotation marks and citations omitted). Despite its goal of broad disclosure, FOIA allows agencies to withhold documents that fit within one of nine exemptions. See 5 U.S.C. § 552(b). In the instant case, the Department of Health and Human Services (“HHS”) invoked Exemptions 6, 7(C), and 7(D) to justify withholding the information requested by Dr. McCutchen. Exemption 6 protects “personnel and medical files and similar files the disclosure of which would constitute a clearly unwarranted invasion of personal privacy.” Id. § 552(b)(6). Exemption 7(C) allows withholding of

records or information compiled for law enforcement purposes, but only to the extent that the production of such law enforcement records or information ... could reasonably be expected to constitute an unwarranted invasion of personal privacy.

Id. § 552(b)(7)(C).

Comparing the language of these two provisions, the Supreme Court has noted:

*185 [W]hereas Exemption 6 requires that the invasion of privacy be “clearly unwarranted,” the adverb “clearly” is omitted from Exemption 7(C) ... [and] whereas Exemption 6 refers to disclosures that “would constitute” an invasion of privacy, Exemption 7(C) encompasses any disclosure that “could reasonably be expected to constitute” such an invasion.

Department of Justice v. Reporters Comm. for Freedom of the Press, 489 U.S. 749, 756, (1989). “Thus, the standard for evaluating a threatened invasion of privacy interests ... is somewhat broader” under Exemption 7(C) than under Exemption 6. Id.

Both Exemptions 6 and 7(C) call for a balancing of “the privacy interests that would be compromised by disclosure against the public interest in release of the requested information.” Beck, 997 F.2d at 1491 (internal quotation marks and citations omitted). On the public interest side of the scale is “the citizens’ right to be informed about what their government is up to.” Id. (internal quotation marks and citations omitted).

Exemption 7(D), which HHS invoked only to justify withholding the complainants’ names, shields “records or information compiled for law enforcement purposes, but only to the extent that the production of such law enforcement records or information ... could reasonably be expected to disclose the identity of a confidential source-” 5 U.S.C. § 552(b)(7)(D).

Under FOIA, the burden is on the agency to justify withholding requested information and the agency’s refusal to disclose it is subject to de novo review by the district court. Id. § 552(a)(4)(B).

B. Office of Scientific Integrity

When this suit was filed in the district court, the Public Health Service Act (“PHSA”), 42 U.S.C. §§ 201 et seq. (1988), required HHS to demand that all applicants for research funding establish “an administrative process to review reports of scientific fraud” and “report to the Secretary [of HHS] any investigation of alleged scientific fraud which appears substantial.” Id. § 289b(a). In addition, the Director of the National Institutes of Health (“NIH”), an HHS official, was required to “establish a process for the prompt and appropriate response to information ... respecting scientific fraud in connection with projects” funded by the PHSA. Id. § 289b(b). In accordance with this mandate, HHS created the Office of Scientific Integrity (“OSI”) to “oversee[ ] the implementation of all ... policies and procedures related to scientific misconduct.” 42 C.F.R. § 50.102. “Misconduct” includes “fabrication, falsification, plagiarism, or other practices that seriously deviate from those that are commonly accepted within the scientific community for proposing, conducting, or reporting research.” Id.

After this suit was filed, Congress amended the PHSA, see National Institutes of Health Revitalization Act of 1993, Pub.L. No. 103-43 § 161 (1993); and HHS abolished OSI, transferring its functions to the Office of the Assistant Secretary for Health, see 57 Fed.Reg. 24,262 (1992). While still extant, however, OSI investigated research performed within NIH as well as research performed at outside institutions that receive PHSA funds, such as universities. Allegations of misconduct involving research by a recipient institution could be investigated by that institution or by OSI. OSI supervised all investigations conducted by outside institutions, however, and could perform its own inquiry if not satisfied. If OSI found misconduct, it could recommend sanctions, including disciplinary action against government researchers and termination of funding and debarment from future grants for outside researchers.

C. Procedural History

On February 7, 1990, Dr.

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30 F.3d 183, 308 U.S. App. D.C. 121, 1994 U.S. App. LEXIS 20250, Counsel Stack Legal Research, https://law.counselstack.com/opinion/dr-charles-w-mccutchen-appelleecross-appellant-v-us-department-of-cadc-1994.