California Moth Specimens: Browse by County

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"The drift of spray from pesticide applications can expose people, wildlife and the environment to pesticide residues that can cause health and environmental effects and property damage." US EPA

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A History of Secret Human Experiments by date.

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In 1997 and again in 2000,
U.S. Title 50, Section 32 was
actually revised to allow for exceptions in conducting experiments on unwitting
citizens.

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Army Tests Bio-Weapons
on U.S. Citizens short
factual video.

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Death in the Air:
Globalism, Terrorism & Toxic Warfare - by Leonard G. Horowitz, D.M.D., M.A., M.P.H.
Death in the Air presents a hard-hitting and factual survey of widespread global abuses
in public health; the links between globalism and genocide; new concepts in "nonlethal" biological
and chemical warfare.

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What Do We Mean by Human Studies?
The definitions of "research" and of "human subjects " in the Common Rule are very broad and embrace many different types of studies among them epidemiology studies, observational studies, and studies involving intentional exposure of human subjects.
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US EPA-United States Environmental Protection Agency says "scientific studies have linked particulate matter,... with a series of significant health problems, including: Premature death."
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Title 40: Protection of Environment PART 26—PROTECTION OF HUMAN SUBJECTS:

TITLE 40 (source)

PART 26--PROTECTION OF HUMAN SUBJECTS

Subpart A--BASIC EPA POLICY FOR PROTECTION OF SUBJECTS IN HUMAN RESEARCH CONDUCTED OR SUPPORTED BY EPA

§26.101 To what does this policy apply? §26.102 Definitions.

§26.103 Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency.

§§26.104-26.106 [Reserved]

§26.107 IRB membership.

§26.108 IRB functions and operations.

§26.109 IRB review of research.

§26.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.

§26.111 Criteria for IRB approval of research.

§26.112 Review by institution.

§26.113 Suspension or termination of IRB approval of research.

§26.114 Cooperative research.

§26.115 IRB records.

§26.116 General requirements for informed consent.

§26.117 Documentation of informed consent.

§26.118 Applications and proposals lacking definite plans for involvement of human subjects.

§26.119 Research undertaken without the intention of involving human subjects.

§26.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency.

§26.121 [Reserved]

§26.122 Use of Federal funds.

§26.123 Early termination of research support: Evaluation of applications and proposals.

§26.124 Conditions.


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Subpart B—Prohibition of Research Conducted or Supported by EPA Involving Intentional Exposure of Human Subjects who are Children or Pregnant or Nursing Women

§26.201 To what does this subpart apply?

§26.202 Definitions.

§26.203 Prohibition of research conducted or supported by EPA involving intentional exposure of any human subject who is a pregnant woman (and therefore her fetus), a nursing woman, or child.