605 F.2d 673 (3rd Cir. 1979), 78-2203, Dow Chemical Co. v. United States E.P.A.
|Citation:||605 F.2d 673|
|Party Name:||The DOW CHEMICAL COMPANY, Petitioner, v. UNITED STATES ENVIRONMENTAL PROTECTION AGENCY and Douglas Costle, Administrator, Respondents.|
|Case Date:||August 24, 1979|
|Court:||United States Courts of Appeals, Court of Appeals for the Third Circuit|
Argued June 8, 1979.
[Copyrighted Material Omitted]
Robert V. Zener, Pepper, Hamilton & Scheetz, Washington, D. C., James S. Hanson, Midland, Mich., for petitioner.
James W. Moorman, Asst. Atty. Gen., Land & Natural Resources Div., Angus MacBeth, Chief, Pollution Control Sec., Michael P. Carlton (Argued), Atty., Dept. of Justice, Washington, D. C., Joan Z. Bernstein, Gen. Counsel, Alan H. Carpien (Argued), Atty., Environmental Protection Agency, Washington, D. C., for respondents.
Before ADAMS, and ROSENN, Circuit Judges, and LACEY, District Judge. [*]
ADAMS, Circuit Judge.
One of the assumptions upon which our society is premised is that technological advancement will be encouraged and material comfort will be increased by rewarding innovation with profit. Long ago, Sir Edward Coke noted that "everyone thirsteth after gaine," 1 and, by and large, the law recognizes that experimentation and innovation will be persisted in only to the degree that an opportunity for "gaine" is presented. 2 This may be especially so today when our continued efforts in scientific research depend almost as much on those who are willing to fund them as on the ingenuity of the researchers themselves.
But the recognition of the desirability of encouraging technological advancement does not mean that the Congress, if it chooses to do so, may not diminish innovation to some degree in order to further some other purpose. Nor does it mean that courts may refuse to give effect to such a legislative decision even if they suspect that the "other purpose" guiding the legislature will be disserved rather than furthered by the statute in question. This is so because Congress is entitled to make its own judgments in this area and once they are made the judiciary must respect them even if its own assessments are to the contrary.
I. DOW'S CHALLENGE TO THE EPA'S INTERPRETATION OF SECTION 8(d) OF TOXIC SUBSTANCES CONTROL ACT.
The present appeal is by Dow Chemical Company, which charges that the Environmental Protection Agency (EPA) is misread its statutory mandate in seeking, under § 8(d) of the Toxic Substances Control Act, 15 U.S.C. § 2607(d) (1976), to obtain information and studies regarding research and development projects undertaken by a commercial enterprise, when such research and development are ultimately expected to produce a profitable product. Section 8(d) provides:
(d) Health and safety studies. The Administrator shall promulgate rules under which the Administrator shall require any person who manufactures, processes, or distributes in commerce or who proposes to manufacture, process, or distribute in commerce any chemical substance or mixture (or with respect to paragraph (2), any person who has possession of a study) to submit to the Administrator
(1) lists of health and safety studies (A) conducted or initiated by or for such person with respect to such substance or mixture at any time, (B) known to such person, or (C) reasonably ascertainable by such person, except that the Administrator may exclude certain types or categories of studies from the requirements of this subsection if the Administrator finds that submission of lists of such studies are
unnecessary to carry out the purposes of this Act; and
(2) copies of any study contained on a list submitted pursuant to paragraph (1) or otherwise known by such person.
Guidance in interpreting § 8 is provided by the following definition in subsection (f):
"For purposes of this section, the terms 'manufacture' and 'process' mean manufacture or process for commercial purposes." The dispute in the case at hand concerns the scope of the authority given the Administrator under § 8.
Congress passed the Toxic Substances Control Act, 15 U.S.C. §§ 2601-2629 (1976), in order to prevent the general environment from becoming the laboratory in which harmful effects of chemicals are discovered. The Act establishes an intricate and at times unfathomable system of regulation administered by the EPA. It places the burden of ensuring adequate research and testing of toxic substances squarely on those companies who seek to profit from the use or sale of such chemicals.
One of the most important provisions of the Act is § 4, which gives the Administrator the authority to require that certain companies those that manufacture, distribute in commerce, process, use, or dispose of chemical substances or mixtures that the EPA suspects may be hazardous conduct tests on such materials. 15 U.S.C. § 2603(a). Section 4(e) calls for the establishment of a committee that is expected to make recommendations to the EPA regarding what chemicals or mixtures should be tested pursuant to § 4(a). This committee, known as the Interagency Testing Committee (I.T.C.), is required to publish in the Federal Register and transmit to the EPA a list of chemicals and proposed areas of study.
In October 1977 the I.T.C. published such a list, including ten chemicals and categories of chemicals. 42 Fed.Reg. 55026. According to the I.T.C. list, the specified chemicals presented serious potential for public exposure and there was a substantial possibility that they could be hazardous. The Committee recommended testing in six general areas: carcinogenicity, mutagenicity, teratogenicity, other chronic effects, environmental effects, and epidemiology. 3
To determine what tests would be necessary, the EPA, pursuant to § 8(d), proposed a rule designed to obtain the submission of already existing health and safety studies. 4 This proposed regulation stipulated that all manufacturers, processors and distributors of any of the named chemicals must submit to the EPA lists of studies initiated by or conducted for them and copies of any such studies in their possession. Section 1(a)(4) of EPA's proposed rule defined the terms "manufacture or process" to include all manufacture or process of chemicals even if only for research purposes. 5
Several interested parties commented on § 1(a)(4) of the proposed rule, complaining that submission to the EPA of information gleaned from tests for new uses of chemicals might discourage product research and development inasmuch as competitors would be apt to gain valuable information about a company's future plans. 6 Notwithstanding these complaints, the changes made in the final rule gave no relief to
those troubled by the possible chilling effects of the regulation on product research and development and innovation in the chemical field generally. Instead, the Agency specifically included a "Note" in the final regulation stating that the definition of manufacturing "for commercial purposes" includes "product research and development." 43 Fed.Reg. 39086. And the two principal changes made to the proposed rule broadened rather than narrowed the scope of the regulation.
Most important for our purposes, the final rule required that the companies subject to the rule submit copies of health and safety studies in their possession even if the studies were of chemicals that that company did not manufacture, process, or distribute. The listing requirement itself, however, remained limited to those substances actually manufactured, processed or distributed by the reporting company. See 40 C.F.R. § 730.5(a), 43 Fed.Reg. 30986. A second change substantially expanded the scope of the type of studies sought beyond the six areas suggested by the I.T.C.
Dow, believing the changes in the proposed rule to be significant, charged that the EPA had violated the Administrative Procedure Act by enlarging the scope of the regulation without adequate notice and fair opportunity to comment. See 5 U.S.C. § 553 (1976). Dow also challenged the Administrator's substantive authority under the Act in two respects. First, it contended that the manufacture of small quantities of a chemical solely for purposes of research and development is Not manufacture "for commercial purposes" and, therefore, is beyond the reach of § 8(d). Second, Dow urged that the EPA's effort to obtain copies of studies under § 8(d)(2) should be limited to those studies that a company was required to list under § 8(d)(1). The second paragraph, Dow argued, cannot be read to give the Agency a power broader than that given in the first paragraph.
In apparent response to Dow's filing of a petition and brief on December 15, 1978, the EPA, on January 26, 1979, withdrew the rule. But the EPA still insists that the regulation was within its statutory authority and that it was revoked solely because of procedural irregularities. Given the revocation, however, the EPA maintains that Dow's appeal is now moot inasmuch as it challenges a rule that is no longer in effect. Before we may consider the merits of Dow's petition, then, we must first address the question of mootness a question that implicates the jurisdiction of the Court.
At first reading, the case for dismissing the present petition as moot has considerable appeal. Simply put, the government urges that there is at this time no rule extant with which Dow must comply. Moreover, the government asserts there is no suggestion that Dow failed to comply in any material respect with the now-withdrawn rule when that rule was in effect. Thus, it may fairly be questioned whether this litigation retains the characteristics of a live case or controversy necessary for adjudication in a federal court. A careful analysis persuades us, however, that the petition is not moot.
In recent years the Supreme Court has evolved a mootness doctrine that includes both constitutional 7 and policy 8 elements. Under Article III, section 2 of the Constitution, the...
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