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The Federal "Data
Quality Act" Is Our Friend...
Opinion by Consumer Advocate
Tim
Bolen
Saturday,
August 27th, 2011
It is no secret that I constantly sell
the idea that an alliance needs to be
made between the North American Health
Freedom Movement and the Autism
communities. I keep pointing out
that each community, having operated on
their own for years, have developed
strategies and tactics that serve them
well.
My best argument, made to the Health
Freedom Movement, FOR that alliance is
simple: I point out that the
Autism community is the best public
example of what happens when a social,
in this case medical, system goes bad,
and stays bad - an issue we fight every
day in Health Freedom. I also
point out that the Autism community is
LARGE and ANGRY. Then too, Autism
seems to be an affliction of the Upper
Middle Class - people who do not take
"no" for an answer - and they generally
are of the opinion that the government
works for them - not the other way
around. Just like us.
My best argument to the Autism
community, FOR that alliance is that the
Health Freedom movement has separate
components that work together, we have a
very good track record, we are
experienced, and we are used to dealing
with the human filth that inhabits the
formal opposition. We know when to
put on a biohazard suit, and go into the
fray with fumigation equipment, so to
speak.
In middle March of 2007 I got a call
from Anne Dachel from Age of Autism (AOA)
asking me why I hadn't done any articles
on the Autism problem. My answer
was direct: Because, Anne, I said,
"I don't know anything about the
issue."
What evolved from that was a
collaboration between
Kenneth Stoller, MD, FAAP and Anne
Dachel to write two superb articles for
my newsletter:
"Throwing
children into oncoming traffic: The
truth about Autism"
and
"The
Mushroom Cloud that Caused Autism".
You can read those by clicking on the
titles.
Coming to the
point...
So, when Ken Stoller MD calls me at home
at 8:30 PM at night to talk to me about
my latest Autism article
"Vaccines - The
Emperor Has No Clothes...," I
take the call. Ken is a fountain
of information.
Ken's comments on my article centered
around what's called the "Data
Quality Act" and its prospective use
in the situation I described surrounding
the State Department's issuance of an
unsigned, un-accounted-for, document to
the United Nations Environmental
Programme (UNEP) on mercury claiming
that mercury was no problem in
vaccinations.
I suggest you read, carefully, the
linked article
"Federal Agencies Subject
to Data Quality Act"
-
By
Susan M. Bisong of
Modrall Sperling. But, for
now, let me give you the gist of what
you are going to read, because this is a
powerful tool for us to use:
"The Data Quality
Act (DQA) is an attempt by Congress to ensure that
federal agencies use and disseminate accurate
information. The DQA requires federal agencies to
issue information quality guidelines ensuring the
quality, utility, objectivity and integrity of
information that they disseminate and provide
mechanisms for affected persons to correct such
information. It is important for natural resources
and environmental attorneys to be aware of this law
in the event that a client has an interest in filing
a petition with an agency to challenge the quality
of information it has used or disseminated.
Questions that remain unanswered about the DQA are
whether agency information quality guidelines apply
to rule-making and whether an agency's denial of a
petition to correct information is reviewable by the
courts.
I. Background
Information
In 1980, Congress
enacted the Paperwork Reduction Act (PRA) in
response to the federal government's growing demand
for data from small businesses, individuals, and
state and local governments and attempted to
institute controls over government requests for
data. 44 U.S.C. § 3501(1). Under the PRA, Congress
established the Office of Information and Regulatory
Affairs (OIRA) within the Office of Management and
Budget (OMB) and designated it as the overseer of
other federal agencies with respect to paperwork. 44
U.S.C. § 3503(a) and (b). The OIRA is responsible
for developing uniform policies for efficient
information processing, storage, and transmittal
systems, both within and among agencies. Id.
The DQA, which is
uncodified, amends the PRA. 44 U.S.C. 3501 et seq.
It was enacted in December of 2000 as a
two-paragraph provision buried in an appropriations
bill. See Treasury and General Government
Appropriation Act for Fiscal Year 2001, Pub. L. No.
106-554, § 515 Appendix C, 114 Stat. 2763A-153
(2000) (attached to the back of this memo). The DQA
took effect on October 1, 2002, the deadline for
federal agencies to issue their final information
quality guidelines.
II. Purpose of the
Data Quality Act
Congress enacted
the DQA primarily in response to increased use of
the internet, which gives agencies the ability to
communicate information easily and quickly to a
large audience. Under the DQA, federal agencies must
ensure that the information it disseminates meets
certain quality standards. Congress' intent was to
prevent the harm that can occur when government
websites, which are easily and often accessed by the
public, disseminate inaccurate information. See
Guidelines for Ensuring and Maximizing the Quality,
Objectivity, Utility, and Integrity of Information
Disseminated by Federal Agencies; Republication, 67
F.R. 8452, 8452 (Feb. 22, 2002).[1]"
There is a lot more to read - especially
for those of us contemplating its use.
So how does the
"Data
Quality Act"
actually work?
That's the question. Despite my
intent, last night, to go to bed early
and read the DQA material in the
morning, Ken had my attention, and I
began to read. Time flew by.
The most interesting article on the
subject I found was about the use of
the DQA in the enactment of the
Endangered Species Act (ESA). ESA
management, as required, established an
ESA DQA program (see how quickly I
can fall into government alphabet
jargon?) called
"The purposes,
effects, and future of the Endangered
Species Act's best available science
mandate."
The key statement here is the "best
available science mandate" phrase in
the title. Think how that phrase,
forced on the vaccine construction,
would impact the vaccine debate.
Just below I will give you the outline
for the Endangered Species Act plan to
follow DQA guidelines. Imagine
applying this outline to the vaccine
argument.
I. INTRODUCTION
II. THE BEST AVAILABLE SCIENCE
MANDATE
A. Overview of the Endangered Species Act
B. The Best Available Science Mandate: Statutory and
Regulatory
Requirements for Consideration of
Science and Observation of
Scientific Norms
1. Statutory Requirements
2. Implementing Regulations and
Policies
III. A BRIEF TAXONOMY OF STANDARDS FOR
SCIENTIFIC DATA
A. Research Science: Replication and Review
B. Courtroom Science: Relevance and Reliability
C. Regulatory Science: "Sound Science, " Precautionary
Principle,
or Agency Discretion?
IV. THE FUNCTIONS OF THE ESA's
BEST AVAILABLE SCIENCE MANDATE
A. The Intent Behind the Best Available Science Mandate
B. The Effects of the Best Available Science Mandate in
Practice
1. Substantive Decision Making
a. Why
Science is Net Enough
b. Why
the Best Available Science Mandate Plays
Only a
Limited Substantive Role
2. Public Trust and Political
Accountability
3. Altering the Terms of Judicial
Review
4. Changing the Decision-Making
Process
V. MAKING THE BEST OF THE
BEST AVAILABLE SCIENCE MANDATE
A. Openly Acknowledge the Limits of Science
B. Increase the Knowledge Base
C. Build Public Trust
VI. CONCLUSION
Would the "best available science
mandate" mean, for instance, that we
would NOT have to suffer though another
so-called study where a small bunch of
bureaucrats, along with their
"stakeholders," claim to REVIEW
other studies - like the one written
about in the New York Times just the
other day? Where was the science
in that?
The most disappointing article I
found on the subject talks about the
two lawsuits against federal agencies
that failed to force the agencies to
change their so-called science.
The courts, so far, have decided that
they, the courts, do not have
jurisdiction to enforce the DQA.
Too bad.
However, I read, carefully, the appeals
court decisions - and sooner or later
some law firm is going to get the
argument formula exactly right, and that
will be the day that federal agencies
will be forced to comply. Agencie,
I think, from my reading, know this is
coming, and are complying more, and
more, with the DQA requirements.
So, to me, now is the time to
start hammering certain agencies with
compliance demands.
Attorney
Paul S. Weiland,
of Nossman LLP, I thinks says it
best in his article
"Data Quality Act Provides Under-utilized Tool to Challenge Federal Agency Use of Faulty Information; Four Years After its Enactment Effect of Act Remains Unclear."
He says:
"Irrespective of the ultimate view of the courts
regarding judicial review of agency responses to
requests for correction of information, the
administrative procedure mandated by Congress in the
DQA and implemented by OMB and the federal agencies
provides stakeholders with a formalized opportunity
to ask agencies to evaluate the quality of
information they disseminate. Whereas existing
administrative and environmental laws provide
stakeholders with an opportunity to engage agencies
at prescribed intervals during agency
decision-making processes (for example, the
Administrative Procedure Act, Endangered Species
Act, National Environmental Policy Act, and National
Forest Management Act), the DQA provides
stakeholders with an opportunity to seek correction
of information at any time along the decision-making
continuum. This supplemental opportunity to
establish a dialog with federal agencies may prove a
valuable procedural device to individuals and
organizations that are affected by agency
activities."
Paul Weiland has litigated environmental matters in
trial and appellate courts under a variety of
statutes, including the Clean Water Act, Endangered
Species Act, and National Environmental Policy Act.
And, Guess
What? The US State Department Has
an Established DQA Program...
You can read it by clicking
here.
One more thing.
You can reach Ken Stoller MD at 8:30 PM,
or even later, by clicking
here, or
here.
Stay tuned.
Tim Bolen - Consumer
Advocate
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