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Clinical Reference Materials Survey - Google Forms
NIST Clinical Reference Materials Survey
The mission of the National Institute of Standards and Technology (NIST) is to serve the clinical and
industrial community by advancing measurement science, standards, and technology. One way we do
so is by providing primary reference materials, which are defined as materials that are certified to be
traceable to the international system of units (SI). In an effort to evaluate and prioritize which materials
are needed within the clinical community, we have designed a reference materials survey. We value
your input, so please take a few minutes to answer the questions below.
Thank you for your time!
* Required
1. 1) Which company or testing laboratory do you
represent? *
2. 2) What best describes your affiliation? *
Mark only one oval.
Private
Government
Academia
Industry
3. 3) What is your perception of the purpose of a primary reference material?
You may choose more than one response.
Check all that apply.
as a positive control for diagnostic testing
as a calibrant for kit manufacturing
as a calibrant for a positive control
extraction control only
detection control only
full extraction through detection control
everyday use control
Other:
4. 4) Do you use primary reference materials in your work? *
Mark only one oval.
Yes
No
Unsure
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5. 5) If yes to question 4, from where do you purchase your reference materials?
You may choose more than one response.
Check all that apply.
Acrometrix
Advanced Biotechnologies
Institute for Reference Materials and Measurements (IRMM)
Maine Molecular Quality Controls
National Institute for Biological Standards and Controls (NIBSC)
National Institute of Standards and Technology (NIST)
World Health Organization (WHO)
Zeptometrix
Other:
6. 6) For what purposes do you use primary reference materials?
You may choose more than one response.
Check all that apply.
as a positive control for diagnostic testing
as a calibrant for kit manufacturing
as a calibrant for a positive control
extraction control only
detection control only
full extraction through detection control
everyday use control
Other:
7. 7) For which viruses, microbes, cancers, genetic diseases, or other disease/organism does
your laboratory or company currently use reference materials?
8. 8) Do you think that primary reference materials are a necessity in the clinical community? *
Mark only one oval.
Yes
No
Unsure
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9. 9) What is your preferred matrix (specimen type) for a reference material? *
You may choose more than one response.
Check all that apply.
Cells
Viral Particles
Urine
Serum/Plasma
Blood
Extracted DNA or RNA in a buffer
Other:
10. 10) If a reference material in your preferred matrix is unavailable, would extracted DNA/RNA in
a buffer work for your purposes? *
Mark only one oval.
Yes
No
Unsure
11. 11) If you work with viruses, would you rather have multiple materials of different genotypes
of a virus or one material with a conserved region of the viral genome?
Mark only one oval.
Multiple materials of different genotypes
One material with a conserved region
Other:
12. 12) If you answered, "multiple genotypes" to question 11, please explain.
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13. 13) What other primary reference materials do you think the clinical community lacks?
Please prioritize in order of importance and be specific (eg - DNA construct with mutations for X
disease or genome for Y).
14. 14) We would love to hear any other comments or suggestions here.
Please feel free to leave your contact info or contact me directly as well (email on the next page).
Thank you for your feedback! Please hit "submit" below!
This collection of information contains Paperwork Reduction Act (PRA) requirements approved by the
Office of Management and Budget (OMB, Control #0693-0033, expiration date 03/31/16).
Notwithstanding any other provisions of the law, no person is required to respond to, nor shall any person
be subject to a penalty for failure to comply with, a collection of information subject to the requirements
of the PRA unless that collection of information displays a currently valid OMB control number. Public
reporting burden for this collection is estimated to be 10 minutes per response, including the time for
reviewing instructions, searching existing data sources, gathering and maintaining the data needed and
completing and reviewing the collection of information.
Send comments regarding this burden estimate or any aspect of this collection of information, including
suggestions for reducing this burden, to the National Institute of Standards and Technology, Attn: Dr. Jo
Lynne Harenza, [email protected].
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File Type | application/pdf |
File Title | Clinical Reference Materials Survey - Google Forms |
File Modified | 2014-07-08 |
File Created | 2014-07-07 |