U DOT Drug And Alcohol Ing Management Information System (MIS) Data Collection Form

User Manual: DOT Drug and Alcohol ing Management Information System (MIS) Data Collection Form

Open the PDF directly: View PDF PDF.
Page Count: 11

DownloadU DOT Drug And Alcohol Ing Management Information System (MIS) Data Collection Form
Open PDF In BrowserView PDF
Appendix H to Part 40 –
DOT Drug and Alcohol Testing Management Information System (MIS) Data Collection Form

U.S. DEPARTMENT OF TRANSPORTATION DRUG AND ALCOHOL TESTING MIS DATA COLLECTION FORM

Calendar Year Covered by this Report: ________________

OMB No. 2105-0529

I. Employer:
Company Name:
Doing Business As (DBA) Name (if applicable):
Address:_______________________________________________________________________________ E-mail: ________________________
Signature: _________________________________________________

Name of Certifying Official:

Telephone: (_____)______________________________________ Date Certified: ___________________________________________________
Prepared by (if different): ________________________________________________________ Telephone: (_____)________________________
C/TPA Name and Telephone (if applicable): __________________________________________________ (_____)________________________
Check the DOT agency for which you are reporting MIS data; and complete the information on that same line as appropriate:
___ FMCSA – Motor Carrier: DOT #: ______________________ Owner-operator: (circle one) YES or NO Exempt (Circle One) YES or NO
___ FAA – Aviation: Certificate # (if applicable): _______________________ Plan / Registration # (if applicable):___________________________
___ RSPA – Pipeline: (Check) Gas Gathering__ Gas Transmission__ Gas Distribution__ Transport Hazardous Liquids__ Transport Carbon Dioxide__
___ FRA – Railroad: Total Number of observed/documented Part 219 “Rule G” Observations for covered employees: __________________________
___ USCG – Maritime: Vessel ID # (USCG- or State-Issued): ______________________________________ (If more than one vessel, list separately.)
___ FTA – Transit
II. Covered Employees: (A) Enter Total Number Safety-Sensitive Employees In All Employee Categories:
(B) Enter Total Number of Employee Categories:
(C)

Employee Category

If you have multiple employee categories, complete Sections I
and II (A) & (B). Take that filled-in form and make one copy
for each employee category and complete Sections II (C), III,
and IV for each separate employee category.

Total Number of Employees
in this Category

III. Drug Testing Data:
3

4

5

6

7

8

9

10

11

12

13

Pre-Employment
Random
Post-Accident
Reasonable Susp./Cause
Return-to-Duty
Follow-Up
TOTAL

Pre-Employment
Random
Post-Accident
Reasonable Susp./Cause
Return-to-Duty
Follow-Up
TOTAL

4

5

6

7

8

9

Cancelled Results

Other Refusals
To Submit To
Testing

“Shy Lung” ~
With No Medical
Explanation

Confirmation Tests
With Results 0.04 Or
Greater

Confirmation Tests
With Results 0.02
Through 0.039

Refusal Results
Number Of
Confirmation Tests
Results

3
Screening Tests With
Results 0.02 Or
Greater

2
Screening Tests With
Results Below 0.02

Type of Test

1
Total Number Of
Screening Test
Results [Should equal
the sum of Columns
2, 3, 7, and 8]

IV. Alcohol Testing Data:

Cancelled Results

Other Refusals To
Submit To
Testing

“Shy Bladder” ~
With No Medical
Explanation

Substituted

Adulterated

Positive For
Amphetamines

Positive For
Opiates

Positive For
PCP

Positive For
Cocaine

Positive For
Marijuana

Verified Positive
Results ~ For One Or
More Drugs

Refusal Results
Verified Negative
Results

Type of Test

2

Total Number Of Test
Results [Should equal
the sum of Columns 2,
3, 9, 10, 11, and 12]

1

PAPERWORK REDUCTION ACT NOTICE (as required by 5 CFR 1320.21)
According to the Paperwork Reduction Act of 1995, no persons are required to respond to a
collection of information unless it displays a valid OMB control number. The valid OMB control
number for this information collection is 2105-0529. The Department of Transportation estimates
that the average burden for this report form is 1.5 hours. You may send comments regarding this
burden estimate or any suggestions for reducing the burden to: U.S. Department of Transportation,
Office of Drug and Alcohol Policy and Compliance, Room 10403, 400 Seventh Street, SW,
Washington, D.C. 20590; OR Office of Management and Budget, Paperwork Reduction Project,
725 Seventeenth Street, NW, Washington, D.C. 20503.

Title 18, USC Section 1001, makes it a criminal offense subject to a maximum fine of $10,000, or
imprisonment for not more than 5 years, or both, to knowingly and willfully make or cause to be
made any false or fraudulent statements of representations in any matter within the jurisdiction of
any agency of the United States.

U.S. DEPARTMENT OF TRANSPORTATION
DRUG AND ALCOHOL TESTING MIS DATA COLLECTION FORM
INSTRUCTION SHEET
This Management Information System (MIS) form is made-up of four sections: employer information; covered
employees (i.e., employees performing DOT regulated safety-sensitive duties) information; drug testing data; and
alcohol testing data. The employer information needs only to be provided once per submission. However, you
must submit a separate page of data for each employee category for which you report testing data. If you are
preparing reports for more than one DOT agency then you must submit DOT agency-specific forms.
Please type or print entries legibly in black ink.
TIP ~ Read the entire instructions before starting. Please note that USCG-regulated employers do not report
alcohol test results on the MIS form.
Calendar Year Covered by this Report: Enter the appropriate year.
Section I. Employer
1. Enter your company’s name, to include when applicable, your “doing business as” name; current address, city,
state, and zip code; and an e-mail address, if available.
2. Enter the printed name, signature, and complete telephone number of the company official certifying the accuracy
of the report and the date that person certified the report as complete.
3. If someone other than the certifying official completed the MIS form, enter that person’s name and phone number
on the appropriate lines provided.
4. If a Consortium/Third Party Administrator (C/TPA) performs administrative services for your drug and alcohol
program operation, enter its name and phone number on the appropriate lines provided.
5. DOT Agency Information: Check the box next to the DOT agency for which you are completing this MIS form.
Again, if you are submitting to multiple DOT agencies, you must use separate forms for each DOT agency.
a. If you are completing the form for FMCSA, enter your FMCSA DOT Number, as appropriate. In addition, you
must indicate whether you are an owner-operator (i.e., an employer who employs only himself or herself as a driver)
and whether you are exempt from providing MIS data. Exemptions are noted in the FMCSA regulation at
382.103(d).
b. If you are completing the form for FAA, enter your FAA Certificate Number and FAA Antidrug Plan /
Registration Number, when applicable.
c. If you are completing the form for RSPA, check the additional box(s) indicating your type of operation.
d. If you are completing the form for FRA, enter the number of observed/documented Part 219 “Rule G”
Observations for covered employees.
e. If you are submitting the form for USCG, enter the vessel ID number. If there is more than one number, enter the
numbers separately.
Section II. Covered Employees
1. In Box II-A, enter the total number of covered employees (i.e., employees performing DOT regulated safetysensitive duties) who work for your company. Then enter, in Box II-B, the total number of employee categories
that number represents. If you have employees, some of whom perform duties under one DOT agency and others of
whom perform duties under another DOT agency, enter only the number of those employees performing duties
under the DOT agency for whom you are submitting the form. If you have covered employees who perform multiDOT agency functions (e.g., an employee drives a commercial motor vehicle and performs pipeline maintenance
duties for you), count the employee only on the MIS report for the DOT agency regulating more than 50 percent of
the employee’s safety sensitive function.

1

[Example: If you are submitting the information for the FRA and you have 2000 covered employees performing
duties in all FRA-covered service categories – you would enter “2000” in the first box (II-A) and “5” in the second
box (II-B), because FRA has five safety-sensitive employee categories and you have employees in all of these
groups. If you have 1000 employees performing safety-sensitive duties in three FRA-covered service categories
(e.g., engine service, train service, and dispatcher/operation), you would enter “1000” in the first box (II-A) and “3”
in the second box (II-B).]
TIP ~ To calculate the total number of covered employees, add the total number of covered employees eligible for
testing during each random testing selection period for the year and divide that total by the number of random
testing periods. (However, no company will need to factor the average number of employees more often than once
per month). For instance, a company conducting random testing quarterly needs to add the total of covered
employees they had in the random pool when each selection was made; then divide this number by 4 to obtain the
yearly average number of covered employees. It is extremely important that you place all eligible employees into
these random pools. [As an example, if Company A had 1500 employees in the first quarter random pool, 2250 in
the second quarter, 2750 in the third quarter; and 1500 in the fourth quarter; 1500 + 2250 + 2750 + 1500 = 8000;
8000 / 4 = 2000; the total number of covered employees for the year would be reported as,“2000”.
If you conduct random selections more often than once per month (e.g., you select daily, weekly, bi-weekly), you do
not need to compute this total number of covered employees rate more than on a once per month basis. Therefore,
employers need not compute the covered employees rate more than 12 times per year.]
2. If you are reporting multiple employee categories, enter the specific employee category in box II-C; and provide
the number of employees performing safety-sensitive duties in that specific category.
[Example: You are submitting data to the FTA and you have 2000 covered employees. You have 1750 personnel
performing revenue vehicle operation and the remaining 250 are performing revenue vehicle and equipment
maintenance. When you provide vehicle operation information, you would enter “Revenue Vehicle Operation” in
the first II-C box and “1750” in the second II-C box. When you provide data on the maintenance personnel, you
would enter “Revenue Vehicle and Equipment Maintenance” in the first II-C box and “250” in the second II-C box.]
TIP ~ A separate form for each employee category must be submitted. You may do this by filling out a single MIS
form through Section II-B and then make one copy for each additional employee category you are reporting. [For
instance, if you are submitting the MIS form for the FMCSA, you need only submit one form for all FMCSA covered
employees working for you – your only category of employees is “driver.” If you are reporting testing data to the
FAA and you employ only flight crewmembers, flight attendants, and aircraft maintenance workers, you need to
complete one form each for category – three forms in all. If you are reporting to FAA and have all FAA categories
of covered employees, you must submit eight forms.]
Here is a full listing of covered-employee categories:
FMCSA (one category): Driver
FAA (eight categories): Flight Crewmember; Flight Attendant; Flight Instructor; Aircraft Dispatcher; Aircraft
Maintenance; Ground Security Coordinator; Aviation Screener; Air Traffic Controller
RSPA (one category): Operation/Maintenance/Emergency Response
FRA (five categories): Engine Service; Train Service; Dispatcher/Operation; Signal Service; Other [Includes
yardmasters, hostlers (non-engineer craft), bridge tenders; switch tenders, and other miscellaneous employees
performing 49 CFR 228.5 (c) defined covered service.]
USCG (one category): Crewmember
FTA (five categories): Revenue Vehicle Operation; Revenue Vehicle and Equipment Maintenance; Revenue Vehicle
Control/Dispatch; CDL/Non-Revenue Vehicle; Armed Security Personnel

2

Section III. Drug Testing Data
This section summarizes the drug testing results for all covered employees (to include applicants). The table in this
section requires drug test data by test type and by result. The categories of test types are: Pre-Employment;
Random; Post-Accident; Reasonable Suspicion / Reasonable Cause; Return-to-Duty, and Follow-Up.
The categories of type of results are: Total Number of Test Results [excluding cancelled tests and blind specimens];
Verified Negative; Verified Positive; Positive for Marijuana; Positive for Cocaine; Positive for PCP; Positive for
Opiates; Positive for Amphetamines; Refusals due to Adulterated, Substituted, “Shy Bladder” with No Medical
Explanation, and Other Refusals to Submit to Testing; and Cancelled Results.
TIP ~ Do not enter data on blind specimens submitted to laboratories. Be sure to enter all pre-employment testing
data regardless of whether an applicant was hired or not. You do not need to separate reasonable suspicion and
reasonable cause drug testing data on the MIS form. [Therefore, if you conducted only reasonable suspicion drug
testing (i.e., FMCSA and FTA), enter that data; if you conducted only reasonable cause drug testing (i.e., FAA,
RSPA, and USCG); or if you conducted both under FRA drug testing rules, simply enter the data with no
differentiation.] For USCG, enter any “Serious Marine Incident” testing in the Post-Accident row. For FRA, do
not enter post accident data (the FRA does not collect this data on the MIS form). Finally, you may leave blank any
row or column in which there were no results, or you may enter “0” (zero) instead. Please note that cancelled tests
are not included in the “total number of test results” column.
Section III, Column 1. Total Number of Test Results ~ This column requires a count of the total number of test
results in each testing category during the entire reporting year. Count the number of test results as the number of
testing events resulting in negative, positive, and refusal results. Do not count cancelled tests and blind specimens
in this total.
[Example: A company that conducted fifty pre-employment tests would enter “50” on the Pre-Employment row. If
it conducted one hundred random tests, “100’ would be entered on the Random row. If that company did no postaccident, reasonable suspicion, reasonable cause, return-to-duty, or follow-up tests, those categories will be left
blank or zeros entered.]
Section III, Column 2. Verified Negative Results ~ This column requires a count of the number of tests in each
testing category that the Medical Review Officer (MRO) reported as negative. Do not count a negative-dilute result
if, subsequently, the employee underwent a second collection; the second test is the test of record.
[Example: If forty-seven of the company’s fifty pre-employment tests were reported negative, “47” would be
entered in Column 2 on the Pre-Employment row. If ninety of the company’s one hundred random test results were
reported negative, “90” would be entered in Column 2 on the Random row. Because the company did no other
testing, those other categories would be left blank or zeros entered.]
Section III, Column 3. Verified Positive Results ~ For One Or More Drugs ~ This column requires a count of
the number of tests in each testing category that the MRO reported as positive for one or more drugs. When the
MRO reports a test positive for two drugs, it would count as one positive test.
[Example: If one of the fifty pre-employment tests was positive for two drugs, “1” would be entered in Column 3
on the Pre-Employment row. If four of the company’s one hundred random test results were reported positive
(three for one drug and one for two drugs), “4” would be entered in Column 3 on the Random row.]
■ Section III, Columns 4 through 8. Positive (for specific drugs) ~ These columns require entry of the by-drug
data for which specimens were reported positive by the MRO.

3

[Example: The pre-employment positive test reported by the MRO was positive for marijuana, “1” would be
entered in Column 4 on the Pre-Employment row. If three of the four positive results for random testing were
reported by the MRO to be positive for marijuana, “3” would be entered in Column 4 on the Random row. If one of
the four positive results for random testing was reported positive for both PCP and opiates, “1” would be entered in
Column 6 on the Random row and “1” would be entered in Column 7 of the Random row.]
TIP ~ Column 1 should equal the sum of Columns 2, 3, 9, 10, 11, and 12. Remember you have not counted
specimen results that were ultimately cancelled or were from blind specimens. So, Column 1 = Column 2 +
Column 3 + Column 9 + Column 10 + Column 11 + Column 12. Certainly, double check your records to
determine if your actual results count is reflective of all negative, positive, and refusal counts.
An MRO may report that a specimen is positive for more than one drug. When that happens, to use the company
example above (i.e., one random test was positive for both PCP and opiates), the positive results should be
recorded in the appropriate columns – PCP and opiates in this case. There is no expectation for Columns 4
through 8 numbers to add up to the numbers in Column 3 when you report multiple positives.
Section III, Columns 9 through 12. Refusal Results ~ The refusal section is divided into four refusal groups –
they are: Adulterated; Substituted; “Shy Bladder” ~ With No Medical Explanation; and Other Refusals To Submit
to Testing. The MRO reports two of these refusal types – adulterated and substituted specimen results – because of
laboratory test findings.
When an individual does not provide enough urine at the collection site, the MRO conducts or causes to have
conducted a medical evaluation to determine if there exists a medical reason for the person’s inability to provide the
appropriate amount of urine. If there is no medical reason to support the inability, the MRO reports the result to the
employer as a refusal to test: Refusals of this type are reported in the “Shy Bladder” ~ With No Medical
Explanation category.
Finally, additional reasons exist for a test to be considered a refusal. Some examples are: the employee fails to
report to the collection site as directed by the employer; the employee leaves the collection site without permission;
the employee fails to empty his or her pockets at the collection site; the employee refuses to have a required shy
bladder evaluation. Again, these are only four examples: there are more.
■ Section III, Column 9. Adulterated ~ This column requires the count of the number of tests reported by the
MRO as refusals because the specimens were adulterated.
[Example: If one of the fifty pre-employment tests was adulterated, “1” would be entered in Column 9 of the PreEmployment row.]
■ Section III, Column 10. Substituted ~ This column requires the count of the number of tests reported by the
MRO as refusals because the specimens were substituted.
[Example: If one of the 100 random tests was substituted, “1” would be entered in Column 10 of the Random row.]
■ Section III, Column 11. “Shy Bladder” ~ With No Medical Explanation ~ This column requires the count of
the number of tests reported by the MRO as being a refusal because there was no legitimate medical reason for an
insufficient amount of urine.
[Example: If one of the 100 random tests was a refusal because of shy bladder, “1” would be entered in Column 11
of the Random row.]

4

■ Section III, Column 12. Other Refusals To Submit To Testing ~ This column requires the count of refusals
other than those already entered in Columns 9 through 11.
[Example: If the company entered “100” as the number of random specimens collected, however it had five
employees who refused to be tested without submitting specimens: two did not show up at the collection site as
directed; one refused to empty his pockets at the collection site; and two left the collection site rather than submit to
a required directly observed collection. Because of these five refusal events, “5” would be entered in Column 11 of
the Random row.]
TIP ~ Even though some testing events result in a refusal in which no urine was collected and sent to the
laboratory, a “refusal” is still a final test result. Therefore, your overall numbers for test results (in Column 1) will
equal the total number of negative tests (Column 2); positives (Column 3); and refusals (Columns 9, 10, 11, and
12). Do not worry that no urine was processed at the laboratory for some refusals; all refusals are counted as a
testing event for MIS purposes and for establishing random rates.
Section III, Column 13. Cancelled Tests ~ This column requires a count of the number of tests in each testing
category that the MRO reported as cancelled. You must not count any cancelled tests in Column 1 or in any other
column. For instance, you must not count a positive result (in Column 3) if it had ultimately been cancelled for any
reason (e.g., specimen was initially reported positive, but the split failed to reconfirm).
[Example: If a pre-employment test was reported cancelled, “1” would be entered in Column 13 on the PreEmployment row. If three of the company’s random test results were reported cancelled, “3” would be entered in
Column 13 on the Random row.]
TOTAL Line. Columns 1 through 13 ~ This line requires you to add the numbers in each column and provide the
totals.
Section IV. Alcohol Testing Data
This section summarizes the alcohol testing conducted for all covered employees (to include applicants). The table
in this section requires alcohol test data by test type and by result. The categories of test types are: PreEmployment; Random; Post-Accident; Reasonable Suspicion / Reasonable Cause; Return-to-Duty, and Follow-Up.
The categories of results are: Number of Screening Test Results; Screening Tests with Results Below 0.02;
Screening Tests with Results 0.02 Or Greater; Number of Confirmation Test Results; Confirmation Tests with
Results 0.02 through 0.039; Confirmation Tests with Results 0.04 Or Greater; Refusals due to “Shy Lung” with No
Medical Explanation, and Other Refusals to Submit to Testing; and Cancelled Results.
TIP ~ Be sure to enter all pre-employment testing data regardless of whether an applicant was hired or not. Of
course, for most employers pre-employment alcohol testing is optional, so you may not have conducted this type of
testing. You do not need to separate “reasonable suspicion” and “reasonable cause” alcohol testing data on the
MIS form. [Therefore, if you conducted only reasonable suspicion alcohol testing (i.e., FMCSA, FAA, FTA, and
RSPA), enter that data; if you conducted both reasonable suspicion and reasonable cause alcohol testing (i.e..,
FRA), simply enter the data with no differentiation.] RSPA does not authorize “random” testing for alcohol.
Finally, you may leave blank any row or column in which there were no results, or you may enter “0” (zero)
instead. Please note that USCG-regulated employers do not report alcohol test results on the MIS form: Do not
fill-out Section IV if you are a USCG-regulated employer.

5

Section IV, Column 1. Total Number of Screening Test Results ~ This column requires a count of the total
number of screening test results in each testing category during the entire reporting year. Count the number of
screening tests as the number of screening test events with final screening results of below 0.02, of 0.02 through
0.039, of 0.04 or greater, and all refusals. Do not count cancelled tests in this total.
[Example: A company that conducted twenty pre-employment tests would enter “20” on the Pre-Employment row.
If it conducted fifty random tests, “50’ would be entered. If that company did no post-accident, reasonable
suspicion, reasonable cause, return-to-duty, or follow-up tests, those categories will be left blank or zeros entered.]
Section IV, Column 2. Screening Tests With Results Below 0.02 ~ This column requires a count of the number
of tests in each testing category that the BAT or STT reported as being below 0.02 on the screening test.
[Example: If seventeen of the company’s twenty pre-employment screening tests were reported as being below
0.02, “17” would be entered in Column 2 on the Pre-Employment row. If forty-four of the company’s fifty random
screening test results were reported as being below 0.02, “44” would be entered in Column 2 on the Random row.
Because the company did no other testing, those other categories would be left blank or zeros entered.]
Section IV, Column 3. Screening Tests With Results 0.02 Or Greater ~ This column requires a count of the
number of screening tests in each testing category that BAT or STT reported as being 0.02 or greater on the
screening test.
[Example: If one of the twenty pre-employment tests was reported as being 0.02 or greater, “1” would be entered in
Column 3 on the Pre-Employment row. If four of the company’s fifty random test results were reported as being
0.02 or greater, “4” would be entered in Column 3 on the Random row.]
Section IV, Column 4. Number of Confirmation Test Results ~ This column requires entry of the number of
confirmation tests that were conducted by a BAT as a result of the screening tests that were found to be 0.02 or
greater. In effect, all screening tests of 0.02 or greater should have resulted in confirmation tests. Ideally the
number of tests in Column 3 and Column 4 should be the same. However, we know that this required confirmation
test sometimes does not occur. In any case, the number of confirmation tests that were actually performed should
be entered in Column 4.
[Example: If the one pre-employment screening test reported as 0.02 or greater had a subsequent confirmation test
performed by a BAT, “1” would be entered in Column 4 on the Pre-Employment row. If three of the four random
screening tests that were found to be 0.02 or greater had a subsequent confirmation test performed by a BAT, “3”
would be entered in Column 4 on the Random row.]
Section IV, Column 5. Confirmation Tests With Results 0.02 Through 0.039 ~ This column requires entry of
the number of confirmation tests that were conducted by a BAT that led to results that were 0.02 through 0.039.
[Example: If the one pre-employment confirmation test yielded a result of 0.042, Column 5 of the Pre-Employment
row would be left blank or zeros entered. If two of the random confirmation tests yielded results of 0.03 and 0.032,
“2” would be entered in Column 5 of the Random row.]
Section IV, Column 6. Confirmation Tests With Results 0.04 Or Greater ~ This column requires entry of the
number of confirmation tests that were conducted by a BAT that led to results that were 0.04 or greater.
[Example: Because the one pre-employment confirmation test yielded a result of 0.042, “1” would be entered in
Column 6 of the Pre-Employment row. If one of the random confirmation tests yielded a result of 0.04, “1” would
be entered in Column 6 of the Random row.]

6

TIP ~ Column 1 should equal the sum of Columns 2, 3, 7, and 8. The number of screening tests results should
reflect the number of screening tests you have no matter the result (below 0.02 or at or above 0.02, plus refusals to
test), unless of course, the tests were ultimately cancelled. So, Column 1 = Column 2 + Column 3 + Column 7 +
Column 8. Certainly, double check your records to determine if your actual screening results count is reflective of
all these counts.
There is no need to record MIS confirmation tests results below 0.02: That is why we have no column for it on the
form. [If the random test that screened 0.02 went to a confirmation test, and that confirmation test yielded a result
below 0.02, there is no place for that confirmed result to be entered.] We assume that if a confirmation test was
completed but not listed in either Column 5 or Column 6, the result was below 0.02. In addition, if the confirmation
test ended up being cancelled, it should not have been included in Columns 1, 3, or 4 in the first place.
Section IV, Columns 7 and 8. Refusal Results ~ The refusal section is divided into two refusal groups – they are:
Shy Lung ~ With No Medical Explanation; and Other Refusals To Submit to Testing. When an individual does not
provide enough breath at the test site, the company requires the employee to have a medical evaluation to determine
if there exists a medical reason for the person’s inability to provide the appropriate amount of breath. If there is no
medical reason to support the inability as reported by the examining physician, the employer calls the result a
refusal to test: Refusals of this type are reported in the “Shy Lung ~ With No Medical Explanation” category.
Finally, additional reasons exist for a test to be considered a refusal. Some examples are: the employee fails to
report to the test site as directed by the employer; the employee leaves the test site without permission; the
employee fails to sign the certification at Step 2 of the ATF; the employee refuses to have a required shy lung
evaluation. Again, these are only four examples; there are more.
■ Section IV, Column 7. “Shy Lung” ~ With No Medical Explanation ~ This column requires the count of the
number of tests in which there is no medical reason to support the employee’s inability to provide an adequate
breath as reported by the examining physician; subsequently, the employer called the result a refusal to test.
[Example: If one of the 50 random tests was a refusal because of shy lung, “1” would be entered in Column 7 of the
Random row.]
■ Section IV, Column 8. Other Refusals To Submit To Testing ~ This column requires the count of refusals
other than those already entered in Columns 7.
[Example: The company entered “50” as the number of random specimens collected, however it had one employee
who did not show up at the testing site as directed. Because of this one refusal event, “1” would be entered in
Column 8 of the Random row.]
TIP ~ Even though some testing events result in a refusal in which no breath (or saliva) was tested, there is an
expectation that your overall numbers for screening tests (in Column 1) will equal the total number of screening
tests with results below 0.02 (Column 2); screening tests with results 0.02 or greater (Column 3); and refusals
(Columns 7 and 8). Do not worry that no breath (or saliva) was tested for some refusals; all refusals are counted
as a screening test event for MIS purposes and for establishing random rates.
Section IV, Column 9. Cancelled Tests ~ This column requires a count of the number of tests in each testing
category that the BAT or STT reported as cancelled. Do not count any cancelled tests in Column 1 or in any other
column other than Column 9. For instance, you must not count a 0.04 screening result or confirmation result in any
column, other than Column 9, if the test was ultimately cancelled for some reason (e.g., a required air blank was not
performed).

7

[Example: If a pre-employment test was reported cancelled, “1” would be entered in Column 9 on the PreEmployment row. If three of the company’s random test results were reported cancelled, “3” would be entered in
Column 13 on the Random row.]
TOTAL Line. Columns 1 through 9 ~ This line requires you to add the numbers in each column and provide the
totals.

8



Source Exif Data:
File Type                       : PDF
File Type Extension             : pdf
MIME Type                       : application/pdf
PDF Version                     : 1.4
Linearized                      : Yes
Page Count                      : 11
XMP Toolkit                     : XMP toolkit 2.9.1-13, framework 1.6
About                           : uuid:7d2b5d0c-0884-4e47-90e2-1ac41c3d7e7c
Producer                        : Acrobat Distiller 6.0.1 (Windows)
Company                         : DOT
Source Modified                 : D:20040329164622
Headline                        : 
Creator Tool                    : Acrobat PDFMaker 6.0 for Word
Modify Date                     : 2004:03:29 11:48:13-05:00
Create Date                     : 2004:03:29 11:46:46-05:00
Metadata Date                   : 2004:03:29 11:48:13-05:00
Document ID                     : uuid:59f58f81-5868-484b-b061-b484733de58d
Version ID                      : 6
Format                          : application/pdf
Title                           : U
Creator                         : bohdan.baczara
Subject                         : 
Tagged PDF                      : Yes
Author                          : bohdan.baczara
EXIF Metadata provided by EXIF.tools

Navigation menu