39660
. (a) Upon the request of the state board, the office, in
consultation with and with the participation of the state board,
shall evaluate the health effects of and prepare recommendations
regarding substances, other than pesticides in their pesticidal use,
which may be or are emitted into the ambient air of California and
that may be determined to be toxic air contaminants.
(b) In conducting this evaluation, the office shall consider all
available scientific data, including, but not limited to, relevant
data provided by the state board, the State Department of Health
Services, the Occupational Safety and Health Division of the
Department of Industrial Relations, the Department of Pesticide
Regulation, international and federal health agencies, private
industry, academic researchers, and public health and environmental
organizations. The evaluation shall be performed using current
principles, practices, and methods used by public health
professionals who are experienced practitioners in the fields of
epidemiology, human health effects assessment, risk assessment, and
toxicity.
(c) (1) The evaluation shall assess the availability and quality
of data on health effects, including potency, mode of action, and
other relevant biological factors, of the substance, and shall, to
the extent that information is available, assess all of the
following:
(A) Exposure patterns among infants and children that are likely
to result in disproportionately high exposure to ambient air
pollutants in comparison to the general population.
(B) Special susceptibility of infants and children to ambient air
pollutants in comparison to the general population.
(C) The effects on infants and children of exposure to toxic air
contaminants and other substances that have a common mechanism of
toxicity.
(D) The interaction of multiple air pollutants on infants and
children, including the interaction between criteria air pollutants
and toxic air contaminants.
(2) The evaluation shall also contain an estimate of the levels of
exposure that may cause or contribute to adverse health effects. If
it can be established that a threshold of adverse health effects
exists, the estimate shall include both of the following factors:
(A) The exposure level below which no adverse health effects are
anticipated.
(B) An ample margin of safety that accounts for the variable
effects that heterogeneous human populations exposed to the substance
under evaluation may experience, the uncertainties associated with
the applicability of the data to human beings, and the completeness
and quality of the information available on potential human exposure
to the substance. In cases in which there is no threshold of
significant adverse health effects, the office shall determine the
range of risk to humans resulting from current or anticipated
exposure to the substance.
(3) The scientific basis or scientific portion of the method used
by the office to assess the factors set forth in this subdivision
shall be reviewed in a manner consistent with this chapter by the
Scientific Review Panel on Toxic Air Contaminants established
pursuant to Article 5 (commencing with Section 39670). Any person may
submit any information for consideration by the panel, which may
receive oral testimony.
(d) The office shall submit its written evaluation and
recommendations to the state board within 90 days after receiving the
request of the state board pursuant to subdivision (a). The office
may, however, petition the state board for an extension of the
deadline, not to exceed 30 days, setting forth its statement of the
reasons that prevent the office from completing its evaluation and
recommendations within 90 days. Upon receipt of a request for
extension of, or noncompliance with, the deadline contained in this
section, the state board shall immediately transmit to the Assembly
Committee on Rules and the Senate Committee on Rules, for transmittal
to the appropriate standing, select, or joint committee of the
Legislature, a statement of reasons for extension of the deadline,
along with copies of the office's statement of reasons that prevent
it from completing its evaluation and recommendations in a timely
manner.
(e) (1) The state board or a district may request, and any person
shall provide, information on any substance that is or may be under
evaluation and that is manufactured, distributed, emitted, or used by
the person of whom the request is made, in order to carry out its
responsibilities pursuant to this chapter. To the extent practical,
the state board or a district may collect the information in
aggregate form or in any other manner designed to protect trade
secrets.
(2) Any person providing information pursuant to this subdivision
may, at the time of submission, identify a portion of the information
submitted to the state board or a district as a trade secret and
shall support the claim of a trade secret, upon the written request
of the state board or district board. Subject to Section 1060 of the
Evidence Code, information supplied that is a trade secret, as
specified in Section 6254.7 of the Government Code, and that is so
marked at the time of submission, shall not be released to any member
of the public. This section does not prohibit the exchange of
properly designated trade secrets between public agencies when those
trade secrets are relevant and necessary to the exercise of their
jurisdiction if the public agencies exchanging those trade secrets
preserve the protections afforded that information by this paragraph.
(3) Any information not identified as a trade secret shall be
available to the public unless exempted from disclosure by other
provisions of law. The fact that information is claimed to be a trade
secret is public information. Upon receipt of a request for the
release of information that has been claimed to be a trade secret,
the state board or district shall immediately notify the person who
submitted the information, and shall determine whether or not the
information claimed to be a trade secret is to be released to the
public. The state board or district board, as the case may be, shall
make its determination within 60 days after receiving the request for
disclosure, but not before 30 days following the notification of the
person who submitted the information. If the state board or district
decides to make the information public, it shall provide the person
who submitted the information 10 days' notice prior to public
disclosure of the information.
(f) The office and the state board shall give priority to the
evaluation and regulation of substances based on factors related to
the risk of harm to public health, amount or potential amount of
emissions, manner of, and exposure to, usage of the substance in
California, persistence in the atmosphere, and ambient concentrations
in the community. In determining the importance of these factors,
the office and the state board shall consider all of the following
information, to the extent that it is available:
(1) Research and monitoring data collected by the state board and
the districts pursuant to Sections 39607, 39617.5, 39701, and 40715,
and by the United States Environmental Protection Agency pursuant to
paragraph (2) of subsection (k) of Section 112 of the federal act (42
U.S.C. Sec. 7412(k)(2)).
(2) Emissions inventory data reported for substances subject to
Part 6 (commencing with Section 44300) and the risk assessments
prepared for those substances.
(3) Toxic chemical release data reported to the state emergency
response commission pursuant to Section 313 of the Emergency Planning
and Community Right-To-Know Act of 1986 (42 U.S.C. Sec. 11023) and
Section 6607 of the Pollution Prevention Act of 1990 (42 U.S.C. Sec.
13106).
(4) Information on estimated actual exposures to substances based
on geographic and demographic data and on data derived from
analytical methods that measure the dispersion and concentrations of
substances in ambient air.