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pdfAssociation of Public Health Laboratories, Inc.
Informed Consent
Form Approved
OMB No. 0920XXXX
Exp. Date XX/XX/20XX
Purpose of the Study: This survey is being performed for the Centers for Disease Control and Prevention (CDC) and the Association of Public
Health Laboratories (APHL) to understand how laboratories use proficiency testing (PT) and how they perceive its value. This survey will take
approximately 20 minutes to complete.
Incentive for Participating: If you wish, by providing your email address, you will be entered in a drawing for a webinar training session on a
current laboratory topic. Within 60 days of the closing date of the survey, a random drawing will be held using those email addresses. Winners will
be notified via email.
Security Information: All information collected in this survey will be kept in a secure manner. No individual answers will be shared with CDC or
APHL. We ask you to include your unique identifier provided in the survey recruitment letter (or your CLIA certificate number) so that we can
connect your survey answers to demographic data that are already on file and to ensure that only one response per laboratory is received. Your IP
address will NOT be retained.
If you would like to be entered in the drawing to receive free webinar training, at the completion of the survey we will request your email address so
that we can notify you if you win. However, your email address will not be linked with data from your survey. The list of email addresses will be
stored electronically in a password protected file and will only be used to randomly select the raffle winners. After the drawing, that file will be
deleted.
Decision to quit at any time: Participation is voluntary; you are free to withdraw from this survey at any time and you may choose to skip any
questions that you do not wish to answer. The number of questions you answer will not affect your chances of winning one of the webinar trainings.
If at any point you do not want to continue, you can simply leave this website. If you do not click on the “submit" button at the end of the survey,
your answers and participation will not be recorded.
How the findings will be used: The results from the study will be compiled and shared in aggregate as a learning tool, presented at professional
conferences, and potentially published in a professional journal in the field of laboratory science.
Contact information: If you have concerns or questions about this study, please contact [email protected] using the subject line “PT survey.”
Agreement: By clicking the NEXT button and beginning the survey, you acknowledge that you have read this information and agree to participate
in this survey, with the knowledge that you are free to withdraw your participation at any time without penalty.
Public reporting burden of this collection of information is estimated to average 20 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. An agency may not conduct or sponsor, and a person is not required to respond to a collection of information unless it displays a
currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of collection of information, including
suggestions for reducing this burden to CDC/ATSDR Information Collection Review Office, 1600 Clifton Road NE , MS D74, Atlanta, Georgia
30333; ATTN: PRA (0920XXXX).
Welcome
Thank you for taking the time to complete this survey by the Association of Public Health Laboratories (APHL) in
collaboration with the Centers for Disease Control and Prevention (CDC). Your feedback is important for guiding APHL
Other
and CDC in their efforts to understand how proficiency testing (PT) is used in clinical laboratories. The survey should
take approximately 20 minutes of your time. All answers will remain completely anonymous.
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Association of Public Health Laboratories, Inc.
For the purpose of this survey, “proficiency testing” means a Centers for Medicare and Medicaid Services (CMS), approved commercial program that
grades your responses and tells you whether you passed or failed each challenge. Click here for a list of PT programs. This list will open in a
separate window.
*1. Please enter the 8digit number that can be found on the address label of the survey
announcement OR the 10digit CLIA number for your laboratory as indicated on the CLIA
certificate. Please note: an independent contractor will use these numbers to assure that
there is only one response per laboratory and to characterize the demographics of survey
respondents. No government agency (local, state or federal) will have the ability to identify
any individual laboratory nor have access to responses submitted.
Please indicate whether you entered the number on the invitation address label or your
laboratory's CLIA number.
j Number on invitation address label
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j CLIA number
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n
Three Phases of Laboratory Testing
Questions 29 will relate to the Three Phases of Laboratory Testing:
Other
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Association of Public Health Laboratories, Inc.
2. Which of the following steps are taken in your laboratory to process PT samples from
the time they are received until the time results are reported to the PT program? (Check all
that
Other apply).
PreAnalytically, our laboratory:
c Disguises the PT specimen to appear to be a patient sample
d
e
f
g
c Enters the PT specimen into the laboratory information system
d
e
f
g
c Examines and evaluates the condition of the specimen when received
d
e
f
g
Analytically, our laboratory:
c Performs preventive maintenance on instruments to be used for PT analysis immediately prior to testing, even when not required
d
e
f
g
c Recalibrates instruments to be used for PT analysis immediately prior to testing
d
e
f
g
c Repeats questionable PT results according to established criteria for repeating patient samples
d
e
f
g
c Tests the specimen in more than one run and averages results
d
e
f
g
c Tests the specimen multiple times within one run and averages the results
d
e
f
g
c Tests the specimen with the same frequency as a patient sample
d
e
f
g
PostAnalytically, our laboratory
c Discards PT samples immediately after analysis
d
e
f
g
c Discusses PT results with another laboratory for verification before reporting results to the PT program
d
e
f
g
c Retains PT samples for future use after reporting results to the PT program
d
e
f
g
c Sends PT samples to another laboratory for additional testing to confirm the PT result
d
e
f
g
c Sends PT samples to another laboratory for additional testing when our standard operating procedure requires referral for patient testing
d
e
f
g
3. How does your laboratory determine which staff employee performs PT? (Check all that
apply).
c PT is performed by the staff member performing the patient testing on that day
d
e
f
g
c PT is performed by the most experienced staff member
d
e
f
g
c PT is systematically rotated among staff on all shifts
d
e
f
g
c Other (please specify):
d
e
f
g
PreAnalytic Phase
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Association of Public Health Laboratories, Inc.
4. Does your laboratory use PT to identify problems that may occur during the preanalytic
phase of laboratory testing?
j Yes
k
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n
j No
k
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n
PreAnalytic Phase
5. For the preanalytic problems listed below, please tell us how important PT is in
identifying them.
Not Important
Potentially Important
Important
Not Applicable
j
k
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n
j
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n
j
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j
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j
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j
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n
Mislabeled samples
j
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n
j
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n
j
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n
j
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n
Personnel competency
j
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n
j
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n
j
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n
j
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n
Delayed processing of
samples
Determination of
insufficient quantity of
samples needed for testing
Identification of improperly
transported samples
Inappropriate specimen
handling, including
dispensing
Inappropriate storage of
samples
Other (please specify):
Analytic Phase
6. Does your laboratory use PT to identify problems that may occur during the analytic
phase of laboratory testing?
j Yes
k
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n
j No
k
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n
Analytic Phase
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Association of Public Health Laboratories, Inc.
7. For the analytic problems listed below, please tell us how important PT is in identifying
them.
Not Important
Potentially Important
Important
Not Applicable
Calibration errors
j
k
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m
n
j
k
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n
j
k
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n
j
k
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m
n
Imprecision (result
j
k
l
m
n
j
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n
j
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n
j
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n
j
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j
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j
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n
Instrumentation problems
j
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n
j
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n
j
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n
j
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n
Specimen dilution errors, if
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variability)
Incorrect test reagent
storage
applicable to method
Specimen extraction errors,
if applicable to method
Other (please specify):
PostAnalytic Phase
8. Does your laboratory use PT to identify problems that may occur during the post
analytic phase of laboratory testing?
j Yes
k
l
m
n
j No
k
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n
PostAnalytic Phase
9. For the postanalytic problems listed below, please tell us how important PT is in
identifying them.
Not Important
Potentially Important
Important
Not Applicable
j
k
l
m
n
j
k
l
m
n
j
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m
n
j
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n
Incorrect calculations
j
k
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n
j
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n
j
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n
j
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n
Incorrect test result
j
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n
j
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n
j
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n
j
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n
j
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j
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j
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j
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j
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n
j
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n
j
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n
j
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n
Delayed reporting to PT
program
interpretation
Sending tests to the wrong
reference laboratory for
confirmatory testing
Transcription errors
Other (please specify):
Page 5
Association of Public Health Laboratories, Inc.
10. To what degree does your laboratory benefit from performing PT for each of the
following aspects?
Educational:
Can be used as a means of
Not Beneficial
Beneficial
Very Beneficial
Not Applicable
j
k
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n
j
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n
j
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n
j
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j
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j
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j
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j
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j
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j
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j
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n
Not Beneficial
Beneficial
Very Beneficial
Not Applicable
j
k
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n
j
k
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n
j
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n
j
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j
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j
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staff competency
assessment
Opportunity to identify
educational areas needing
improvement
Opportunity to obtain
performance feedback from
programs that offer PT
Provides a source of
continuing education
Technical:
Ability to support
confirmation of suspected
analytical trends and/or
imprecision
Comparison of performance
with other participating
(peer) sites
Instrument comparison
before purchase
Onsite performance
evaluation of newly
implemented assays
Regular, external check on
quality of testing
Troubleshooting assays
(identifying and fixing
problems)
Use information in PT
summary reports to support
recommendations to
managers for methodology
or instrument changes
Verification of assay
performance to meet
clinical needs
Page 6
Association of Public Health Laboratories, Inc.
11. How much of a challenge are the following aspects of performing PT to your
laboratory?
Not Challenging
Challenging
Very Challenging
Not Applicable
j
k
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m
n
j
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n
j
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j
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n
Cost for panel analytes that
are not currently being
assayed in your laboratory
Commercially unavailable
analytes (analytes for which
PT does not exist)
Inability to truly treat PT
samples as patient
specimens
Large number of ungraded
challenges
Matrix problems (interfering
substances in sample)
prevent comparison across
all methods (i.e., limited to
method peer groups)
PT program subscription
cost
PT programs lag behind
advancing technology in
laboratory testing
Staff time involved in the
PT process (i.e.,
purchasing, analyzing
and/or interpreting)
Time required to receive
results from PT programs
12. If your laboratory has multiple analyzers available to conduct testing for a given
analyte, how do you choose which analyzer to use for PT?
j PT is conducted on the analyzer used for routine patient specimen analysis that day
k
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n
j PT is conducted on an analyzer predetermined to have the best analytical performance whether routine specimen analysis is performed
k
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n
on that analyzer or not
j PT is conducted on the analyzer which is least expensive to operate
k
l
m
n
j PT is rotated among analyzers
k
l
m
n
j Not applicable – Laboratory only has one analyzer for all tests
k
l
m
n
j Other (please specify):
k
l
m
n
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Association of Public Health Laboratories, Inc.
13. CLIA requires PT for only a limited number of tests or analytes. Click here for a list of
those analytes.This will open in a separate window. How do you meet the requirements to
verify the accuracy of any test or procedure you perform when PT is not required by CLIA
regulations or your accreditation agency for that analyte or test? (Check all that apply).
c PT is purchased for at least some nonCLIA analytes
d
e
f
g
c Patient specimens are split and analyzed in our laboratory or by a reference or peer laboratory inside our laboratory/hospital laboratory
d
e
f
g
system and results compared
c Patient specimens are split, a specimen is sent to a reference or peer laboratory outside our laboratory/hospital laboratory system for
d
e
f
g
analysis and results are compared with our results
c Performance is verified by analysis of quality control materials with established acceptance ranges
d
e
f
g
c PT is required by our accreditation organization even if it is not required by CLIA
d
e
f
g
c Test results are compared among staff within the laboratory
d
e
f
g
c No action taken when commercial PT is unavailable
d
e
f
g
c Not applicable to our laboratory
d
e
f
g
c Other (please specify):
d
e
f
g
14. When PT results are not graded by the PT program due to lack of consensus or for
some other reason, what steps do you take in your laboratory as a substitute? (Check all
that apply).
c Split patient specimens and analyze them in our laboratory or by a reference or peer laboratory inside our laboratory/ hospital laboratory
d
e
f
g
system and compare results
c Split patient specimens, send a specimen for analysis by a reference or peer laboratory outside our laboratory/hospital laboratory system
d
e
f
g
and compare result with our result
c Reanalyze residual PT material from a previously graded event
d
e
f
g
c Compare your result, when possible, with the majority in your peergroup, even if PT was not graded
d
e
f
g
c This situation has not occurred in our laboratory
d
e
f
g
c Take no action regarding proficiency testing
d
e
f
g
c Other (please specify):
d
e
f
g
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Association of Public Health Laboratories, Inc.
15. Do you purchase PT modules for some analytes or tests even when CLIA does not
require it?
j No
k
l
m
n
j Yes, we purchase for 1 5 analytes
k
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m
n
j Yes, we purchase for 6 10 analytes
k
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n
j Yes, we purchase for 11 – 20 analytes
k
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n
j Yes, we purchase for >21 analytes
k
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n
16. How important are the following reasons for purchasing PT that is not required by
CLIA?
Our accreditation
Not Important
Potentially Important
Important
Not Applicable
j
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n
j
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organization requires us to
perform PT
Our medical director or
laboratory director requires
us to perform PT
PT is used to assess
instrument performance
PT is used to test
competency of testing
personnel
PT is used to track accuracy
of methodology
PT provides a source of
continuing education
PT results are valuable for
identifying problems
Used as a marketing tool
Other (please specify):
Page 9
Association of Public Health Laboratories, Inc.
17. How helpful would the following actions be to improve PT?
Not Helpful
Helpful
Very Helpful
Not Applicable
j
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j
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j
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j
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Provide less PT challenges
j
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n
j
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n
j
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j
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Provide more frequent PT
j
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n
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j
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n
Decrease the time allowed
to perform PT from receipt
of samples to reporting
results
Increase the time allowed
to perform PT from receipt
of samples to reporting
results
Increase the use of digital
images instead of slides or
photographs
Increase the use of slides or
photographs instead of
digital images
Improve the quality of
photographs
Improve PT reporting unit
consistency
Standardize the PT
reporting format
Improve technical
feedback/advice from PT
program
Improve PT program
customer service
Provide more PT
challenges
events
Provide less frequent PT
events
Provide faster return of
results from PT programs
Provide more case study
oriented challenges
Provide samples that better
simulate patient specimens
Other (please specify):
Page 10
Association of Public Health Laboratories, Inc.
18. How important are the following resources with respect to providing information about
PT results, testing, and training?
Not aware of this
Not Important
Potentially Important
Important
Not Applicable
j
k
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n
j
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n
j
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j
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j
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j
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j
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j
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j
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n
j
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n
Scientific publications
j
k
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m
n
j
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l
m
n
j
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n
j
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m
n
j
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n
Teleconferences
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
Web searches
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
Other laboratory
resource
professionals inside the
laboratory
Other laboratory
professionals outside your
laboratory
Centers for Disease Control
and Prevention (CDC)
publications and online
resources
Clinical Laboratory
Improvement Amendments
(CLIA) Proficiency Testing
brochure available from the
Centers for Medicare &
Medicaid Services (CMS)
CLSI GP27 – “Using
Proficiency Testing to
Improve the Clinical
Laboratory”
CLSI GP29 – “Assessment
of Laboratory Tests Where
Proficiency Testing is Not
Available”
CMS surveyors or
Accreditation Organization
Inspectors
Educational Modules
provided by the PT
Program
Professional organization
newsletters
Other (please specify):
19. Does your laboratory perform microbiology testing in your laboratory?
j Yes
k
l
m
n
j No
k
l
m
n
Page 11
Association of Public Health Laboratories, Inc.
20. Does your laboratory report PT results for microbiology to the same level as reported
for your patient testing? For example, if you report patient samples for a particular
organism to species level, do you report PT results the same?
j Yes
k
l
m
n
j Yes, but will report to a lower level occasionally
k
l
m
n
j Sometimes report PT at a higher level than patient samples
k
l
m
n
j No
k
l
m
n
21. Which of the following elements of the patient demographics or history provided with a
PT challenge are needed to process and analyze PT samples appropriately? (Check all
that apply).
c Age
d
e
f
g
c Sex
d
e
f
g
c Specimen source/type/site
d
e
f
g
c Symptom(s)
d
e
f
g
c Gram stain reaction
d
e
f
g
22. According to CLIA regulations microbiology does not have analytes, should changes
be made to microbiology PT grading to allow for monitoring performance over time on a
particular type of test or examination – for example, culture, or susceptibility testing?
j Yes, provide scores for each PT test
k
l
m
n
j No
k
l
m
n
Page 12
Association of Public Health Laboratories, Inc.
23. How important would the following be to improve microbiology PT?
Not Important
Potentially Important
Important
Not Applicable
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
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n
j
k
l
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n
j
k
l
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n
j
k
l
m
n
j
k
l
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n
j
k
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n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
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n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
m
n
j
k
l
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n
j
k
l
m
n
j
k
l
m
n
j
k
l
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n
j
k
l
m
n
j
k
l
m
n
j
k
l
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n
j
k
l
m
n
Improve the quality of
photographs
Improve the quality of
stained slides
Include more susceptibility
testing challenges
Include less susceptibility
testing challenges
Include more emerging or
less common organisms
Include fewer emerging or
less common organisms
Increase the use of digital
images instead of slides or
photographs
Increase the use of slides or
photographs instead of
digital images
Require direct antigen
testing in mycology
Require direct antigen
testing in parasitology
Require susceptibility
testing in mycology
Require susceptibility
testing in virology
24. When you consider the benefits of performing proficiency testing as compared to its
costs, would you characterize it as…
j Clearly worth the costs
k
l
m
n
j Somewhat worth the costs
k
l
m
n
j Neutral
k
l
m
n
j Somewhat more costly than its value
k
l
m
n
j Clearly more costly than its value
k
l
m
n
j No opinion
k
l
m
n
Page 13
Association of Public Health Laboratories, Inc.
25. Do you have an opinion or observation about PT that you would like to share that was
not addressed in the survey?
5
6
26. Please provide your email address so that we can notify you if you win the
teleconference training. This is optional, but you cannot be entered in the drawing if an
email is not provided.
email:
Page 14
File Type | application/pdf |
File Modified | 2013-01-08 |
File Created | 2012-11-22 |