[ RadSafe ] Radiobioassay and FDA Approval
jjc105 at yahoo.com
Fri Mar 2 16:19:16 CST 2012
Stan, et al,
Many years ago, I served in the US Air Force in the Medical Service Corps. My
job was to manage a clinical laboratory that analyzed blood, urine, and other
specimens of human origen. The military policy at the time was to conduct
periodic proficiency testing of laboratories to determine their proficiency.
The results of these proficiency tests were then distributed to all
participating laboratories so they could ascertain how well they were doing, as
compared to other laboratoris and known standards. As I recall, the variation of
results from different laboratories on the same samlples were considerable and
often at significant variance with the known sample. From this experience, I was
impressed with the need for surveillance of testing laboratories to assure that
they were proficient in their analyses. I believe it would be a good policy to
conduct periodic proficiency testing at all clinical laboratories, both
military and civilian.
From: Stan Morton <stan.morton at gel.com>
To: Clayton J Bradt <CJB01 at health.state.ny.us>
Cc: radsafe at health.phys.iit.edu
Sent: Fri, March 2, 2012 8:37:59 AM
Subject: Re: [ RadSafe ] Radiobioassay and FDA Approval
Congress passed the Clinical Laboratory Improvement Amendments (CLIA) in
1988 establishing quality standards for all laboratory testing to ensure the
accuracy, reliability and timeliness of patient test results regardless of
where the test was performed. The Centers for Medicare & Medicaid Services
(CMS) regulates all laboratory testing (except research) performed on humans
in the U.S. through the Clinical Laboratory Improvement Amendments (CLIA).
The objective of the CLIA program is to ensure quality laboratory testing.
CLIA requires all facilities that perform even one test, including waived
tests, on "materials derived from the human body for the purpose of
providing information for the diagnosis, prevention, or treatment of any
disease or impairment of, or the assessment of the health of, human beings"
to meet certain Federal requirements. If a facility performs tests for these
purposes, it is considered a laboratory under CLIA and must apply and obtain
a certificate from the CLIA program that corresponds to the complexity of
FDA 'approval' remains a cloud concept whose origin seems to be unknown. I
do know that FDA has implemented new quality control regulations concerning
the preparations of all PET nuclides produced by accelerator technology.
Stan Morton, Manager
GEL Laboratories, LLC
From: Clayton J Bradt [mailto:CJB01 at health.state.ny.us]
Sent: Friday, March 02, 2012 9:17 AM
To: stan.morton at gel.com
Cc: radsafe at health.phys.iit.edu
Subject: re: Radiobioassay and FDA Approval
Stan, what's the difference between "CLIA certification" and "FDA approval"?
Clayton J. Bradt
NYS Dept. of Health
Biggs Laboratory, Room D486A
Empire State Plaza
Albany, NY 12201-0509
It is my personal opinion that the analysis of excreta material is only a
part of the dose-evaluation process. As long as the laboratory reporting
the analytical results does not provide a dose estimate, there is no reason
to require FDA 'approval' should it exist. It should be understood that the
laboratory be required to participate in the appropriate
performance-evaluation programs (i.e., DOELAP, NAVLAP, Oak Ridge, etc.) that
determine ability to provide an acceptable result. I agree the laboratory
should be CLIA certified.
Most HP/MDs that provide dose estimates employ computer programs as part of
the process, i.e. IMBA , DCAL, etc. I know of no program within the FDA
that has the ability to evaluate these codes, or do I know of a program
within FDA that can issue 'approval' to an analytical laboratory to perform
radiobioassay work. In fact, I know of no program in any form that
evaluates the entire dosimetric assessment process. One can see a need.
Manger, Radiobioassay Programs
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