Procedures for Transportation Workplace Drug and Alcohol Testing Programs: Federal Drug Testing Custody and Control Form; Technical Amendment, 59105-59108 [2010-24038]
Download as PDF
Federal Register / Vol. 75, No. 186 / Monday, September 27, 2010 / Rules and Regulations
dates of the clauses in paragraphs
(b)(22) and (c)(2) to read ‘‘(SEP 2010)’’.
■ 4. Section 252.247–7003 is revised to
read as follows:
252.247–7003 Pass-Through of Motor
Carrier Fuel Surcharge Adjustment To The
Cost Bearer.
As prescribed in 247.207, use the
following clause:
PASS-THROUGH OF MOTOR
CARRIER FUEL SURCHARGE
ADJUSTMENT TO THE COST BEARER
(SEP 2010)
(a) This clause implements section 884 of
the National Defense Authorization Act for
Fiscal Year 2009 (Pub. L. 110–417).
(b) Unless an exception is authorized by
the Contracting Officer, the Contractor shall
pass through any motor carrier fuel-related
surcharge adjustments to the person,
corporation, or entity that directly bears the
cost of fuel for shipment(s) transported under
this contract.
(c) The Contractor shall insert the
substance of this clause, including this
paragraph (c), in all subcontracts with motor
carriers, brokers, or freight forwarders.
(End of clause)
[FR Doc. 2010–23664 Filed 9–24–10; 8:45 am]
BILLING CODE 5001–08–P
DEPARTMENT OF TRANSPORTATION
Office of the Secretary
49 CFR Part 40
[Docket DOT–OST–2010–0161]
RIN 2105–AE03
Procedures for Transportation
Workplace Drug and Alcohol Testing
Programs: Federal Drug Testing
Custody and Control Form; Technical
Amendment
Office of the Secretary, DOT.
Interim Final rule.
AGENCY:
ACTION:
The Department of Health and
Human Services recently issued a new
Federal Drug Testing Custody and
Control Form for use in both the Federal
employee and Department of
Transportation drug testing programs. In
order to accommodate the form’s use
within our transportation industry
program, the Department is making a
few necessary regulation changes in
order for collectors, laboratories, and
Medical Review Officers to know how
to use the new form. The form’s use is
authorized beginning October 1, 2010.
The Department is also making a
technical amendment to its drug testing
procedures. The purpose of the
technical amendment is to add a
mstockstill on DSKH9S0YB1PROD with RULES
SUMMARY:
VerDate Mar<15>2010
16:28 Sep 24, 2010
Jkt 220001
provision of the rule which was
inadvertently omitted from the final rule
in August 2010.
DATES: The rule is effective October 1,
2010. Comments to this interim final
rule should be submitted by October 27,
2010. Late-filed comments will be
considered to the extent practicable.
ADDRESSES: To ensure that you do not
duplicate your docket submissions,
please submit them by only one of the
following means:
• Federal eRulemaking Portal: Go to
https://www.regulations.gov and follow
the online instructions for submitting
comments.
• Mail: Docket Management Facility,
U.S. Department of Transportation, 1200
New Jersey Ave., SE., West Building
Ground Floor Room W12–140,
Washington, DC 20590–0001;
• Hand Delivery: West Building
Ground Floor Room W12–140, 1200
New Jersey Ave., SE., between 9 a.m.
and 5 p.m., Monday through Friday,
except Federal holidays. The telephone
number is 202–366–9329;
Instructions: You must include the
agency name and docket number DOT–
OST–2010–0161 or the Regulatory
Identification Number (2105–AE03) for
the rulemaking at the beginning of your
comments. All comments received will
be posted without change to https://
www.regulations.gov, including any
personal information provided.
FOR FURTHER INFORMATION CONTACT:
Bohdan Baczara, U.S. Department of
Transportation, Office of Drug and
Alcohol Policy and Compliance, 1200
New Jersey Avenue, SE., Washington,
DC 20590; 202–366–3784 (voice), 202–
366–3897 (fax), or
bohdan.baczara@dot.gov (e-mail).
SUPPLEMENTARY INFORMATION:
Background
All urine specimens collected under
the Department of Transportation (DOT)
drug testing regulation, 49 CFR Part 40,
must be collected using chain-ofcustody procedures that incorporate the
use of the Federal Drug Testing Custody
and Control Form (CCF) promulgated by
the Department of Health and Human
Services (HHS). On November 17, 2009,
HHS published a proposal to revise the
CCF. [74 FR 59196] All the comments
submitted were thoroughly reviewed by
HHS and taken into consideration in
fashioning the new CCF. The
Department worked closely with HHS
on the new CCF. Recently, HHS
announced the new CCF in the Federal
Register [75 FR 41488] which has an
effective date of October 1, 2010.
The following items in the revised
CCF are worth noting for the DOT
PO 00000
Frm 00049
Fmt 4700
Sfmt 4700
59105
transportation industry drug testing
program:
(1) In Step 1 of the CCF, the Federal
testing authorities—HHS; DOT; and
Nuclear Regulatory Commission
(NRC)—are noted, with further
specificity for the DOT Agencies—
Federal Motor Carrier Safety
Administration (FMCSA); Federal
Aviation Administration (FAA); Federal
Railroad Administration (FRA); Federal
Transit Administration (FTA); Pipeline
and Hazardous Materials Safety
Administration (PHMSA); and the
United States Coast Guard (USCG) 1—
also noted;
(2) In Step 5A on Copy 1 of the CCF,
the new drug analytes MDMA, MDA,
and MDEA are added, as are ‘‘D9–
THCA’’ after ‘‘Marijuana Metabolite’’ and
‘‘BZE’’ after ‘‘Cocaine Metabolite’’ to
specify the drug analytes;
(3) In Step 6 on Copy 2 of the CCF,
a line has been included on which the
Medical Review Officer (MRO) would
write the drug for which a positive
result is verified, and a new line item
‘‘other’’ was added to assist the MRO in
documenting other ‘‘refusal to test’’
situations—for example, when there is
no legitimate medical explanation for
the employee providing an insufficient
amount of urine;
(4) In Step 7 on Copy 2 of the CCF,
a box has been added for the MRO to
check if the split specimen is reported
as cancelled; and
(5) On the reverse side of Copy 5—the
‘‘Donor Copy’’—of the CCF, are the
revised instructions for completing the
CCF.
Because HHS sought and received
comments on the form and its use, we
seek only to receive comments on the
actual implementation of the new CCF,
and not on the form itself.
In addition, the technical amendment
is intended to address an omission
which has been called to our attention
since the publication of the
Department’s final rule in August 2010
[75 FR 49850] which was intended to
create consistency with many of the
new drug testing requirements
established by HHS. Specifically, the
HHS Guidelines require laboratories to
report the concentration of the drug or
drug metabolite for a positive result to
the MRO. This was omitted from our
rule text in the section that directs what
laboratories are to report and how they
are to report it. We have amended the
rule text to reflect this requirement.
1 For purposes of following the requirements of
49 CFR Part 40, ‘‘DOT, The Department, DOT
Agency’’ is defined, at 40.3, to include the United
States Coast Guard.
E:\FR\FM\27SER1.SGM
27SER1
59106
Federal Register / Vol. 75, No. 186 / Monday, September 27, 2010 / Rules and Regulations
mstockstill on DSKH9S0YB1PROD with RULES
Implementation Guidance
DOT-regulated employers and their
service agents are authorized to begin
use of the new CCF on October 1, 2010.
However, we recognize there will be
large supplies of old CCFs available
after the start date. To avoid wasting the
old forms, the Department will permit
use of the old CCF until September 30,
2011. After this date, collectors and
laboratories are not to use any of the old
CCFs in the DOT testing program. The
rule text has been changed to reflect this
one-full-year transition period from old
CCF to new CCF.
However, when the old CCF is used
on or before September 30, 2011, the
collector will need to write in the
specific DOT Agency under which the
specimen is collected and must do so in
the remarks section in Step 2 on Copy
1 of the CCF. This DOT Agency
designation is a new feature in the new
CCF. So, if an old CCF is used and the
employee’s specimen is collected under,
for example, authority of the FMCSA
regulation, the collector will write in
‘‘DOT—FMCSA’’ in the remarks section
in Step 2 of the CCF.
Likewise, when an old CCF is used on
or before September 30, 2011, before
transmitting a confirmed positive drug
test for MDMA, MDA, or MDEA, as
appropriate, to the MRO, the
laboratory—in addition to checking the
‘‘positive’’ box—must write in the
specific MDMA, MDA, or MDEA analyte
in the ‘‘Remarks’’ section in Step 5–A of
Copy 1 of the CCF.
Like now, use of a CCF past its
expiration date will not be a fatal flaw.
Use of the old CCF after September 30,
2011, must be corrected using the
procedures at § 40.205(b)(2).
Regarding the completion of the new
Step 1–D of the CCF, the Department
would like to emphasize that neither the
employer nor the collector should find
it difficult to complete this new data
item. DOT-regulated employers and
their Consortium/Third Party
Administrators (C/TPAs) currently
provide the collector and the collection
site with specific instructions—the test
reason, whether the test is to be
conducted under direct observation, the
MRO name and address, and employee
information (e.g., name and SSN or ID
number), among others. Adding one
additional data element to what is
already provided by employers or their
C/TPAs to collectors should not prove
significantly difficult. An employer and
its C/TPA should be readily aware of the
DOT Agency regulating the employee’s
safety-sensitive duties. We have added a
new § 40.14 to put into one place the
items that employers and their C/TPAs
VerDate Mar<15>2010
16:28 Sep 24, 2010
Jkt 220001
have been routinely providing
collectors, and if they have not been
doing so, the information they should
have always been providing collectors,
in addition to this new requirement for
DOT Agency designations.
If the information in Step 1–D of the
CCF is not completed, the laboratory
will not delay testing the specimen and
reporting the confirmed result to the
MRO. Similarly, the MRO will not delay
the medical review process and
reporting the verified result to the
employer. The Department believes the
laboratory and MRO should note that
the testing authority box was not
checked and continue with processing,
testing, verifying, and reporting the
specimen result, as appropriate. To
reduce the potential failure of the
collector to check the appropriate box in
Step 1–D, the Department will permit
the checkmark to be pre-printed in the
appropriate box prior to the collection.
We amended our rule text to reflect
these situations.
As more of the DOT Agencies go
toward having employee drug testing
violations reported to them, these
designations will prove invaluable to
the process.
Regarding Step 6 of Copy 2 of the
CCF, HHS provided more space for
identifying the positive drug(s) and a
new line item ‘‘Other’’ was added to
assist the MRO in documenting other
‘‘Refusal to Test’’ situations—for
example, when there is no legitimate
medical explanation for the employee
providing an insufficient amount of
urine. In Step 7 of Copy 2 of the CCF,
HHS added a box for ‘‘Test Cancelled’’
for the MRO to check when a test is
cancelled if a split specimen fails to
reconfirm. We amended our rule text to
reflect these modifications. As a
reminder to MROs, the ‘‘Test Cancelled’’
box should only be used when the split
fails to reconfirm for all the results
verified and reported for the primary
specimen.
In light of the modifications HHS
made to Step 7 of Copy 2 of the CCF,
we have taken this opportunity to
incorporate into § 40.187(f) rule text on
how MROs are to document split
specimen results. It is our
understanding that MROs have been
completing this section correctly even
though the rule text did not instruct the
MRO to check the ‘‘Reconfirmed’’
and/or ‘‘Failed to Reconfirm’’ boxes. The
amendment to § 40.187(f) makes this a
requirement.
On the back of Copy 5—the ‘‘Donor
Copy’’—of the CCF, the instructions to
the collector on completing the CCF are
revised and updated.
PO 00000
Frm 00050
Fmt 4700
Sfmt 4700
Regulatory Analyses and Notices
Authority
The statutory authority for this rule
derives from the Omnibus
Transportation Employee Testing Act of
1991 (49 U.S.C. 102, 301, 322, 5331,
20140, 31306, and 54101 et seq.) and the
Department of Transportation Act (49
U.S.C. 322).
Administrative Procedure Act
The Department has determined this
rule may be issued without a prior
opportunity for notice and comment
because providing prior notice and
comment would be unnecessary,
impracticable, or contrary to the public
interest. This rule will authorize DOTregulated employers to use the CCF
beginning October 1, 2010. Providing an
opportunity for prior notice and
comment would be unnecessary, and
would seem redundant, because the
public already had an opportunity to
comment and did provide comments to
HHS on the proposed CCF. In their
Notice of Proposed Revisions to the
Federal Custody and Control Form, HHS
stated that the CCF is used for the
Federal workplace drug testing program
but also pointed out that ‘‘* * * the
Department of Transportation (DOT)
requires its regulated industries to use
the Federal CCF.’’ [74 FR 59196]
Because many of the commenters were
transportation industry employers,
C/TPAs, and associations, we are
confident they understood that the new
CCF would be used in the DOTregulated program. And, because the
DOT utilizes the CCF for our drug
testing program, the DOT and HHS
collaborated in preparing the final CCF.
Providing an opportunity for prior
notice and comment would be
impracticable because there is such a
short time frame from when HHS
published the new CCF [75 FR 41488]
to its October 1, 2010 effective date. In
addition, this Interim Final Rule makes
minor procedural amendments to its
rule text to merely reflect the changes to
the revised CCF and a technical
amendment to correct an inadvertent
oversight from a prior rulemaking. For
these reasons, the Department finds
there is good cause to make the rule
effective immediately.
Executive Order 12866 and Regulatory
Flexibility Act
This Interim Final Rule is not
significant for purposes of Executive
Order 12866 or the DOT’s regulatory
policies and procedures. The rule makes
minor procedural amendments to its
rule text to merely reflect the changes to
the revised CCF and a technical
E:\FR\FM\27SER1.SGM
27SER1
Federal Register / Vol. 75, No. 186 / Monday, September 27, 2010 / Rules and Regulations
amendment to correct an inadvertent
oversight. The use of the revised CCF
does not increase costs on regulated
parties because it authorizes regulated
employers to continue using the old
CCF for an additional twelve months,
until September 30, 2011. After this
date, the revised CCF must be used.
This allows employers to use their
current supply of old CCFs rather than
discarding them. The rule will impose
no new burdens on any parties. While
small entities are among those who may
use the revised CCF, the Department
certifies, under the Regulatory
Flexibility Act, that this rule does not
have a significant economic impact on
a substantial number of small entities.
List of Subjects in 49 CFR Part 40
Issued September 20, 2010, at Washington,
DC.
Ray LaHood,
Secretary of Transportation.
For reasons discussed in the
preamble, the Department of
Transportation amends Title 49 of the
Code of Federal Regulations, Part 40, as
follows:
■
PART 40—PROCEDURES FOR
TRANSPORTATION WORKPLACE
DRUG AND ALCOHOL TESTING
PROGRAMS
1. The authority citation for 49 CFR
part 40 continues to read as follows:
■
Authority: 49 U.S.C. 102, 301, 322, 5331,
20140, 31306, and 54101 et seq.
2. A new § 40.14 is added, to read as
follows:
■
mstockstill on DSKH9S0YB1PROD with RULES
§ 40.14 What collection information must
employers provide to collectors?
As an employer, or an employer’s
service agent—for example a C/TPA,
you must ensure the collector has the
following information when conducting
a urine specimen collection for you:
(a) Full name of the employee being
tested.
(b) Employee SSN or ID number.
(c) Laboratory name and address (can
be pre-printed on the CCF).
(d) Employer name, address, phone
number, and fax number (can be preprinted on the CCF at Step 1–A).
(e) DER information required at
§ 40.35 of this part.
(f) MRO name, address, phone
number, and fax number (can be preprinted on the CCF at Step 1–B).
16:28 Sep 24, 2010
Jkt 220001
§ 40.23 What actions do employers take
after receiving verified test results?
*
Administrative practice and
procedures, Alcohol abuse, Alcohol
testing, Drug abuse, Drug testing,
Laboratories, Reporting and
recordkeeping requirements, Safety,
Transportation.
VerDate Mar<15>2010
(g) The DOT Agency which regulates
the employee’s safety-sensitive duties
(the checkmark can pre-printed in the
appropriate box on the CCF at Step
1–D).
(h) Test reason, as appropriate: Preemployment; Random; Reasonable
Suspicion/Reasonable Cause; PostAccident; Return-to-Duty; and Followup.
(i) Whether the test is to be observed
or not (see § 40.67 of this part).
(j) (Optional) C/TPA name, address,
phone, and fax number (can be preprinted on the CCF).
■ 3. In § 40.23, paragraph (f)(4) is
revised, to read as follows:
*
*
*
*
(f) * * *
(4) You must instruct the collector to
note on the CCF the same reason (e.g.,
random test, post-accident test) and
DOT Agency (e.g., check DOT and
FMCSA) as for the original collection.
*
*
*
*
*
■ 4. In § 40.45, revise paragraphs (b) and
(c)(3), to read as follows:
§ 40.45 What form is used to document a
DOT urine collection?
*
*
*
*
*
(b) You must not use a non-Federal
form or an expired CCF to conduct a
DOT urine collection. As a laboratory,
C/TPA or other party that provides CCFs
to employers, collection sites, or other
customers, you must not provide copies
of an expired CCF to these participants.
You must also affirmatively notify these
participants that they must not use an
expired CCF (e.g., that after September
30, 2011, they may not use an expired
CCF for DOT urine collections).
(c) * * *
(3) As an employer, in Step 1–D of the
CCF you may preprint the box for the
DOT Agency under whose authority the
test will occur.
*
*
*
*
*
■ 5. In § 40.63, paragraph (e) is revised,
to read as follows:
§ 40.63 What steps does the collector take
in the collection process before the
employee provides a urine specimen?
*
*
*
*
*
(e) You must pay careful attention to
the employee during the entire
collection process to note any conduct
that clearly indicates an attempt to
tamper with a specimen (e.g., substitute
urine in plain view or an attempt to
bring into the collection site an
adulterant or urine substitute). If you
detect such conduct, you must require
that a collection take place immediately
PO 00000
Frm 00051
Fmt 4700
Sfmt 4700
59107
under direct observation (see § 40.67)
and complete Step 2 by noting the
conduct in the ‘‘Remarks’’ line of the
CCF and the fact that the collection was
observed by checking the ‘‘Observed’’
box. You must also, as soon as possible,
inform the DER and collection site
supervisor that a collection took place
under direct observation and the reason
for doing so.
■ 6. In § 40.83, paragraph (a) is revised,
to read as follows:
§ 40.83 How do laboratories process
incoming specimens?
*
*
*
*
*
(a) You are authorized to receive only
Copy 1 of the CCF. You are not
authorized to receive other copies of the
CCF or any copies of the alcohol testing
form.
*
*
*
*
*
■ 7. In § 40.97, paragraphs (a)(2)(i) and
(ii), and (e)(1) are revised, to read as
follows:
§ 40.97 What do laboratories report and
how do they report it?
(a) * * *
(2) * * *
(i) Positive, with drug(s)/metabolite(s)
noted, with numerical values for the
drug(s) or drug metabolite(s).
(ii) Positive-dilute, with drug(s)/
metabolite(s) noted, with numerical
values for the drug(s) or drug
metabolite(s) and with numerical values
for creatinine and specific gravity;
*
*
*
*
*
(e) * * *
(1) You must provide quantitative
values for confirmed positive drug test
results to the MRO.
*
*
*
*
*
■ 8. In § 40.129, paragraph (c) is revised,
to read as follows:
§ 40.129 What are the MRO’s functions in
reviewing laboratory confirmed nonnegative drug test results?
*
*
*
*
*
(c) With respect to verified positive
test results, place a checkmark in the
‘‘Positive’’ box in Step 6 on Copy 2 of the
CCF, indicate the drug(s)/metabolite(s)
verified positive, and sign and date the
verification statement.
*
*
*
*
*
9. In § 40.163:
a. Paragraph (c)(8) is amended by
removing ‘‘and’’.
■ b. Paragraph (c)(9) is amended by
removing the period at the end and
adding ‘‘; and’’ in its place.
■ c. Paragraph (c)(10) is added.
The addition reads as follows:
■
■
E:\FR\FM\27SER1.SGM
27SER1
59108
Federal Register / Vol. 75, No. 186 / Monday, September 27, 2010 / Rules and Regulations
§ 40.163 How does the MRO report drug
test results?
*
*
*
*
*
(c) * * *
(10) The DOT Agency, if noted on the
CCF.
*
*
*
*
*
10. In § 40.187, paragraph (f) is
revised to read as follows:
■
§ 40.187 What does the MRO do with split
specimen laboratory results?
*
*
*
*
*
(f) For all split specimen results, as
the MRO you must in Step 7 of Copy 2
of the CCF:
(1) Report split specimen test results
by checking the ‘‘Reconfirmed’’ box and/
or the ‘‘Failed to Reconfirm’’ box, or the
‘‘Test Cancelled’’ box, as appropriate.
(2), Enter your name, sign, and date.
(3) Send a legible copy of Copy 2 of
the CCF (or a signed and dated letter,
see § 40.163) to the employer and keep
a copy for your records. Transmit the
document as provided in § 40.167.
*
*
*
*
(d) * * *
(2) As the MRO, you must note the
refusal by checking the ‘‘Refusal to Test’’
box in Step 6 on Copy 2 of the CCF,
checking whether the specimen was
adulterated or substituted and, if
adulterated, noting the adulterant/
reason. If there was another reason for
the refusal, check ‘‘Other’’ in Step 6 on
Copy 2 of the CCF, and note the reason
next to the ‘‘Other’’ box and on the
‘‘Remarks’’ lines, as needed. You must
then sign and date the CCF.
*
*
*
*
*
12. In § 40.193, paragraph (d)(2)(i) is
revised, to read as follows:
■
§ 40.193 What happens when an employee
does not provide a sufficient amount of
urine for a drug test?
*
*
*
*
*
(d) * * *
(2) * * *
(i) Check the ‘‘Refusal to Test’’ box and
‘‘Other’’ box in Step 6 on Copy 2 of the
CCF and note the reason next to the
‘‘Other’’ box and on the ‘‘Remarks’’ lines,
as needed.
*
*
*
*
*
§ 40.209 What procedural problems do not
result in the cancellation of a test and do
not require corrective action?
*
*
*
*
(b) * * *
(1) A minor administrative mistake
(e.g., the omission of the employee’s
middle initial, a transposition of
numbers in the employee’s social
security number, the omission of the
DOT Agency in Step 1–D of the CCF.)
*
*
*
*
*
(9) Personal identifying information is
inadvertently contained on the CCF
(e.g., the employee signs his or her name
on Copy 1); or
*
*
*
*
*
15. In § 40.355, paragraph (l) is
revised, to read as follows:
■
*
*
*
*
(l) In transmitting documents to
laboratories, you must ensure that you
send to the laboratory that conducts
testing only Copy 1 of the CCF. You
must not transmit other copies of the
CCF or any ATFs to the laboratory.
*
*
*
*
*
[FR Doc. 2010–24038 Filed 9–24–10; 8:45 am]
BILLING CODE 4910–9X–P
*
16:28 Sep 24, 2010
Jkt 220001
Positive Train Control Systems
Federal Railroad
Administration (FRA), Department of
Transportation (DOT).
ACTION: Final rule amendments.
AGENCY:
PO 00000
SUMMARY:
Table of
Contents for Supplementary
Information:
I. Introduction and Background
II. Scope of Further Comments Sought
III. Further Comments Filed and FRA’s
Response
A. Removal From PTCIP of Track Segments
Not Yet Implemented With PTC Systems
B. De Minimis Exception
IV. Section-by-Section Analysis
V. Regulatory Impact and Notices
Partially as a consequence and
severity of certain very public accidents,
coupled with a series of other less
publicized accidents, Congress passed
the Rail Safety Improvement Act of 2008
§ 104, Public Law 110–432, 122 Stat.
§ 40.203 What problems cause a drug test
to be cancelled unless they are corrected?
VerDate Mar<15>2010
RIN 2130–AC03
I. Introduction and Background
13. In § 40.203, paragraphs (d)(2) and
(d)(3) are revised, to read as follows:
*
[Docket No. FRA–2008–0132, Notice No. 4]
SUPPLEMENTARY INFORMATION:
14. In § 40.209, paragraphs (b)(1) and
(b)(9) are revised, to read as follows:
■
■
*
49 CFR Part 236
*
*
*
Federal Railroad Administration
FRA is issuing amendments
to the final rule regarding the
development, testing, implementation,
and use of Positive Train Control (PTC)
systems for railroads as mandated by the
Rail Safety Improvement Act of 2008.
With publication of the final rule on
January 15, 2010, FRA sought further
comment on certain specific issues.
These amendments are being made
partially in response to the applicable
comments filed and to further clarify
certain provisions of the final rule.
DATES: The amendments to the final rule
are effective November 26, 2010.
FOR FURTHER INFORMATION CONTACT:
Thomas McFarlin, Office of Safety
Assurance and Compliance, Staff
Director, Signal & Train Control
Division, Federal Railroad
Administration, Mail Stop 25, West
Building 3rd Floor, Room W35–332,
1200 New Jersey Avenue, SE.,
Washington, DC 20590 (telephone:
202–493–6203) (e-mail:
Thomas.McFarlin@dot.gov); or Jason
Schlosberg, Trial Attorney, Office of
Chief Counsel, RCC–10, Mail Stop 10,
West Building 3rd Floor, Room W31–
217, 1200 New Jersey Avenue, SE.,
Washington, DC 20590 (telephone:
202–493–6032) (e-mail:
Jason.Schlosberg@dot.gov).
*
§ 40.191 What is a refusal to take a DOT
drug test, and what are the consequences?
*
DEPARTMENT OF TRANSPORTATION
§ 40.355 What limitations apply to the
activities of service agents?
11. In § 40.191, paragraph (d)(2) is
revised, to read as follows:
■
mstockstill on DSKH9S0YB1PROD with RULES
(d) * * *
(2) The certifying scientist’s signature
is omitted on Copy 1 of the CCF for a
positive, adulterated, substituted, or
invalid test result.
(3) The collector uses a non-Federal
form or an expired CCF for the test. This
flaw may be corrected through the
procedure set forth in § 40.205(b)(2),
provided that the collection testing
process has been conducted in
accordance with the procedures of this
part in an HHS-certified laboratory.
During the period of October 1, 2010–
September 30, 2011, you are not
required to cancel a test because of the
use of an expired CCF. Beginning
October 1, 2011, if the problem is not
corrected, you must cancel the test.
Frm 00052
Fmt 4700
Sfmt 4700
E:\FR\FM\27SER1.SGM
27SER1
Agencies
[Federal Register Volume 75, Number 186 (Monday, September 27, 2010)]
[Rules and Regulations]
[Pages 59105-59108]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-24038]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF TRANSPORTATION
Office of the Secretary
49 CFR Part 40
[Docket DOT-OST-2010-0161]
RIN 2105-AE03
Procedures for Transportation Workplace Drug and Alcohol Testing
Programs: Federal Drug Testing Custody and Control Form; Technical
Amendment
AGENCY: Office of the Secretary, DOT.
ACTION: Interim Final rule.
-----------------------------------------------------------------------
SUMMARY: The Department of Health and Human Services recently issued a
new Federal Drug Testing Custody and Control Form for use in both the
Federal employee and Department of Transportation drug testing
programs. In order to accommodate the form's use within our
transportation industry program, the Department is making a few
necessary regulation changes in order for collectors, laboratories, and
Medical Review Officers to know how to use the new form. The form's use
is authorized beginning October 1, 2010. The Department is also making
a technical amendment to its drug testing procedures. The purpose of
the technical amendment is to add a provision of the rule which was
inadvertently omitted from the final rule in August 2010.
DATES: The rule is effective October 1, 2010. Comments to this interim
final rule should be submitted by October 27, 2010. Late-filed comments
will be considered to the extent practicable.
ADDRESSES: To ensure that you do not duplicate your docket submissions,
please submit them by only one of the following means:
Federal eRulemaking Portal: Go to https://www.regulations.gov and follow the online instructions for submitting
comments.
Mail: Docket Management Facility, U.S. Department of
Transportation, 1200 New Jersey Ave., SE., West Building Ground Floor
Room W12-140, Washington, DC 20590-0001;
Hand Delivery: West Building Ground Floor Room W12-140,
1200 New Jersey Ave., SE., between 9 a.m. and 5 p.m., Monday through
Friday, except Federal holidays. The telephone number is 202-366-9329;
Instructions: You must include the agency name and docket number
DOT-OST-2010-0161 or the Regulatory Identification Number (2105-AE03)
for the rulemaking at the beginning of your comments. All comments
received will be posted without change to https://www.regulations.gov,
including any personal information provided.
FOR FURTHER INFORMATION CONTACT: Bohdan Baczara, U.S. Department of
Transportation, Office of Drug and Alcohol Policy and Compliance, 1200
New Jersey Avenue, SE., Washington, DC 20590; 202-366-3784 (voice),
202-366-3897 (fax), or bohdan.baczara@dot.gov (e-mail).
SUPPLEMENTARY INFORMATION:
Background
All urine specimens collected under the Department of
Transportation (DOT) drug testing regulation, 49 CFR Part 40, must be
collected using chain-of-custody procedures that incorporate the use of
the Federal Drug Testing Custody and Control Form (CCF) promulgated by
the Department of Health and Human Services (HHS). On November 17,
2009, HHS published a proposal to revise the CCF. [74 FR 59196] All the
comments submitted were thoroughly reviewed by HHS and taken into
consideration in fashioning the new CCF. The Department worked closely
with HHS on the new CCF. Recently, HHS announced the new CCF in the
Federal Register [75 FR 41488] which has an effective date of October
1, 2010.
The following items in the revised CCF are worth noting for the DOT
transportation industry drug testing program:
(1) In Step 1 of the CCF, the Federal testing authorities--HHS;
DOT; and Nuclear Regulatory Commission (NRC)--are noted, with further
specificity for the DOT Agencies--Federal Motor Carrier Safety
Administration (FMCSA); Federal Aviation Administration (FAA); Federal
Railroad Administration (FRA); Federal Transit Administration (FTA);
Pipeline and Hazardous Materials Safety Administration (PHMSA); and the
United States Coast Guard (USCG) \1\--also noted;
---------------------------------------------------------------------------
\1\ For purposes of following the requirements of 49 CFR Part
40, ``DOT, The Department, DOT Agency'' is defined, at 40.3, to
include the United States Coast Guard.
---------------------------------------------------------------------------
(2) In Step 5A on Copy 1 of the CCF, the new drug analytes MDMA,
MDA, and MDEA are added, as are ``[Delta]9-THCA'' after ``Marijuana
Metabolite'' and ``BZE'' after ``Cocaine Metabolite'' to specify the
drug analytes;
(3) In Step 6 on Copy 2 of the CCF, a line has been included on
which the Medical Review Officer (MRO) would write the drug for which a
positive result is verified, and a new line item ``other'' was added to
assist the MRO in documenting other ``refusal to test'' situations--for
example, when there is no legitimate medical explanation for the
employee providing an insufficient amount of urine;
(4) In Step 7 on Copy 2 of the CCF, a box has been added for the
MRO to check if the split specimen is reported as cancelled; and
(5) On the reverse side of Copy 5--the ``Donor Copy''--of the CCF,
are the revised instructions for completing the CCF.
Because HHS sought and received comments on the form and its use,
we seek only to receive comments on the actual implementation of the
new CCF, and not on the form itself.
In addition, the technical amendment is intended to address an
omission which has been called to our attention since the publication
of the Department's final rule in August 2010 [75 FR 49850] which was
intended to create consistency with many of the new drug testing
requirements established by HHS. Specifically, the HHS Guidelines
require laboratories to report the concentration of the drug or drug
metabolite for a positive result to the MRO. This was omitted from our
rule text in the section that directs what laboratories are to report
and how they are to report it. We have amended the rule text to reflect
this requirement.
[[Page 59106]]
Implementation Guidance
DOT-regulated employers and their service agents are authorized to
begin use of the new CCF on October 1, 2010. However, we recognize
there will be large supplies of old CCFs available after the start
date. To avoid wasting the old forms, the Department will permit use of
the old CCF until September 30, 2011. After this date, collectors and
laboratories are not to use any of the old CCFs in the DOT testing
program. The rule text has been changed to reflect this one-full-year
transition period from old CCF to new CCF.
However, when the old CCF is used on or before September 30, 2011,
the collector will need to write in the specific DOT Agency under which
the specimen is collected and must do so in the remarks section in Step
2 on Copy 1 of the CCF. This DOT Agency designation is a new feature in
the new CCF. So, if an old CCF is used and the employee's specimen is
collected under, for example, authority of the FMCSA regulation, the
collector will write in ``DOT--FMCSA'' in the remarks section in Step 2
of the CCF.
Likewise, when an old CCF is used on or before September 30, 2011,
before transmitting a confirmed positive drug test for MDMA, MDA, or
MDEA, as appropriate, to the MRO, the laboratory--in addition to
checking the ``positive'' box--must write in the specific MDMA, MDA, or
MDEA analyte in the ``Remarks'' section in Step 5-A of Copy 1 of the
CCF.
Like now, use of a CCF past its expiration date will not be a fatal
flaw. Use of the old CCF after September 30, 2011, must be corrected
using the procedures at Sec. 40.205(b)(2).
Regarding the completion of the new Step 1-D of the CCF, the
Department would like to emphasize that neither the employer nor the
collector should find it difficult to complete this new data item. DOT-
regulated employers and their Consortium/Third Party Administrators (C/
TPAs) currently provide the collector and the collection site with
specific instructions--the test reason, whether the test is to be
conducted under direct observation, the MRO name and address, and
employee information (e.g., name and SSN or ID number), among others.
Adding one additional data element to what is already provided by
employers or their C/TPAs to collectors should not prove significantly
difficult. An employer and its C/TPA should be readily aware of the DOT
Agency regulating the employee's safety-sensitive duties. We have added
a new Sec. 40.14 to put into one place the items that employers and
their C/TPAs have been routinely providing collectors, and if they have
not been doing so, the information they should have always been
providing collectors, in addition to this new requirement for DOT
Agency designations.
If the information in Step 1-D of the CCF is not completed, the
laboratory will not delay testing the specimen and reporting the
confirmed result to the MRO. Similarly, the MRO will not delay the
medical review process and reporting the verified result to the
employer. The Department believes the laboratory and MRO should note
that the testing authority box was not checked and continue with
processing, testing, verifying, and reporting the specimen result, as
appropriate. To reduce the potential failure of the collector to check
the appropriate box in Step 1-D, the Department will permit the
checkmark to be pre-printed in the appropriate box prior to the
collection. We amended our rule text to reflect these situations.
As more of the DOT Agencies go toward having employee drug testing
violations reported to them, these designations will prove invaluable
to the process.
Regarding Step 6 of Copy 2 of the CCF, HHS provided more space for
identifying the positive drug(s) and a new line item ``Other'' was
added to assist the MRO in documenting other ``Refusal to Test''
situations--for example, when there is no legitimate medical
explanation for the employee providing an insufficient amount of urine.
In Step 7 of Copy 2 of the CCF, HHS added a box for ``Test Cancelled''
for the MRO to check when a test is cancelled if a split specimen fails
to reconfirm. We amended our rule text to reflect these modifications.
As a reminder to MROs, the ``Test Cancelled'' box should only be used
when the split fails to reconfirm for all the results verified and
reported for the primary specimen.
In light of the modifications HHS made to Step 7 of Copy 2 of the
CCF, we have taken this opportunity to incorporate into Sec. 40.187(f)
rule text on how MROs are to document split specimen results. It is our
understanding that MROs have been completing this section correctly
even though the rule text did not instruct the MRO to check the
``Reconfirmed'' and/or ``Failed to Reconfirm'' boxes. The amendment to
Sec. 40.187(f) makes this a requirement.
On the back of Copy 5--the ``Donor Copy''--of the CCF, the
instructions to the collector on completing the CCF are revised and
updated.
Regulatory Analyses and Notices
Authority
The statutory authority for this rule derives from the Omnibus
Transportation Employee Testing Act of 1991 (49 U.S.C. 102, 301, 322,
5331, 20140, 31306, and 54101 et seq.) and the Department of
Transportation Act (49 U.S.C. 322).
Administrative Procedure Act
The Department has determined this rule may be issued without a
prior opportunity for notice and comment because providing prior notice
and comment would be unnecessary, impracticable, or contrary to the
public interest. This rule will authorize DOT-regulated employers to
use the CCF beginning October 1, 2010. Providing an opportunity for
prior notice and comment would be unnecessary, and would seem
redundant, because the public already had an opportunity to comment and
did provide comments to HHS on the proposed CCF. In their Notice of
Proposed Revisions to the Federal Custody and Control Form, HHS stated
that the CCF is used for the Federal workplace drug testing program but
also pointed out that ``* * * the Department of Transportation (DOT)
requires its regulated industries to use the Federal CCF.'' [74 FR
59196] Because many of the commenters were transportation industry
employers, C/TPAs, and associations, we are confident they understood
that the new CCF would be used in the DOT-regulated program. And,
because the DOT utilizes the CCF for our drug testing program, the DOT
and HHS collaborated in preparing the final CCF.
Providing an opportunity for prior notice and comment would be
impracticable because there is such a short time frame from when HHS
published the new CCF [75 FR 41488] to its October 1, 2010 effective
date. In addition, this Interim Final Rule makes minor procedural
amendments to its rule text to merely reflect the changes to the
revised CCF and a technical amendment to correct an inadvertent
oversight from a prior rulemaking. For these reasons, the Department
finds there is good cause to make the rule effective immediately.
Executive Order 12866 and Regulatory Flexibility Act
This Interim Final Rule is not significant for purposes of
Executive Order 12866 or the DOT's regulatory policies and procedures.
The rule makes minor procedural amendments to its rule text to merely
reflect the changes to the revised CCF and a technical
[[Page 59107]]
amendment to correct an inadvertent oversight. The use of the revised
CCF does not increase costs on regulated parties because it authorizes
regulated employers to continue using the old CCF for an additional
twelve months, until September 30, 2011. After this date, the revised
CCF must be used. This allows employers to use their current supply of
old CCFs rather than discarding them. The rule will impose no new
burdens on any parties. While small entities are among those who may
use the revised CCF, the Department certifies, under the Regulatory
Flexibility Act, that this rule does not have a significant economic
impact on a substantial number of small entities.
List of Subjects in 49 CFR Part 40
Administrative practice and procedures, Alcohol abuse, Alcohol
testing, Drug abuse, Drug testing, Laboratories, Reporting and
recordkeeping requirements, Safety, Transportation.
Issued September 20, 2010, at Washington, DC.
Ray LaHood,
Secretary of Transportation.
0
For reasons discussed in the preamble, the Department of Transportation
amends Title 49 of the Code of Federal Regulations, Part 40, as
follows:
PART 40--PROCEDURES FOR TRANSPORTATION WORKPLACE DRUG AND ALCOHOL
TESTING PROGRAMS
0
1. The authority citation for 49 CFR part 40 continues to read as
follows:
Authority: 49 U.S.C. 102, 301, 322, 5331, 20140, 31306, and
54101 et seq.
0
2. A new Sec. 40.14 is added, to read as follows:
Sec. 40.14 What collection information must employers provide to
collectors?
As an employer, or an employer's service agent--for example a C/
TPA, you must ensure the collector has the following information when
conducting a urine specimen collection for you:
(a) Full name of the employee being tested.
(b) Employee SSN or ID number.
(c) Laboratory name and address (can be pre-printed on the CCF).
(d) Employer name, address, phone number, and fax number (can be
pre-printed on the CCF at Step 1-A).
(e) DER information required at Sec. 40.35 of this part.
(f) MRO name, address, phone number, and fax number (can be pre-
printed on the CCF at Step 1-B).
(g) The DOT Agency which regulates the employee's safety-sensitive
duties (the checkmark can pre-printed in the appropriate box on the CCF
at Step 1-D).
(h) Test reason, as appropriate: Pre-employment; Random; Reasonable
Suspicion/Reasonable Cause; Post-Accident; Return-to-Duty; and Follow-
up.
(i) Whether the test is to be observed or not (see Sec. 40.67 of
this part).
(j) (Optional) C/TPA name, address, phone, and fax number (can be
pre-printed on the CCF).
0
3. In Sec. 40.23, paragraph (f)(4) is revised, to read as follows:
Sec. 40.23 What actions do employers take after receiving verified
test results?
* * * * *
(f) * * *
(4) You must instruct the collector to note on the CCF the same
reason (e.g., random test, post-accident test) and DOT Agency (e.g.,
check DOT and FMCSA) as for the original collection.
* * * * *
0
4. In Sec. 40.45, revise paragraphs (b) and (c)(3), to read as
follows:
Sec. 40.45 What form is used to document a DOT urine collection?
* * * * *
(b) You must not use a non-Federal form or an expired CCF to
conduct a DOT urine collection. As a laboratory, C/TPA or other party
that provides CCFs to employers, collection sites, or other customers,
you must not provide copies of an expired CCF to these participants.
You must also affirmatively notify these participants that they must
not use an expired CCF (e.g., that after September 30, 2011, they may
not use an expired CCF for DOT urine collections).
(c) * * *
(3) As an employer, in Step 1-D of the CCF you may preprint the box
for the DOT Agency under whose authority the test will occur.
* * * * *
0
5. In Sec. 40.63, paragraph (e) is revised, to read as follows:
Sec. 40.63 What steps does the collector take in the collection
process before the employee provides a urine specimen?
* * * * *
(e) You must pay careful attention to the employee during the
entire collection process to note any conduct that clearly indicates an
attempt to tamper with a specimen (e.g., substitute urine in plain view
or an attempt to bring into the collection site an adulterant or urine
substitute). If you detect such conduct, you must require that a
collection take place immediately under direct observation (see Sec.
40.67) and complete Step 2 by noting the conduct in the ``Remarks''
line of the CCF and the fact that the collection was observed by
checking the ``Observed'' box. You must also, as soon as possible,
inform the DER and collection site supervisor that a collection took
place under direct observation and the reason for doing so.
0
6. In Sec. 40.83, paragraph (a) is revised, to read as follows:
Sec. 40.83 How do laboratories process incoming specimens?
* * * * *
(a) You are authorized to receive only Copy 1 of the CCF. You are
not authorized to receive other copies of the CCF or any copies of the
alcohol testing form.
* * * * *
0
7. In Sec. 40.97, paragraphs (a)(2)(i) and (ii), and (e)(1) are
revised, to read as follows:
Sec. 40.97 What do laboratories report and how do they report it?
(a) * * *
(2) * * *
(i) Positive, with drug(s)/metabolite(s) noted, with numerical
values for the drug(s) or drug metabolite(s).
(ii) Positive-dilute, with drug(s)/metabolite(s) noted, with
numerical values for the drug(s) or drug metabolite(s) and with
numerical values for creatinine and specific gravity;
* * * * *
(e) * * *
(1) You must provide quantitative values for confirmed positive
drug test results to the MRO.
* * * * *
0
8. In Sec. 40.129, paragraph (c) is revised, to read as follows:
Sec. 40.129 What are the MRO's functions in reviewing laboratory
confirmed non-negative drug test results?
* * * * *
(c) With respect to verified positive test results, place a
checkmark in the ``Positive'' box in Step 6 on Copy 2 of the CCF,
indicate the drug(s)/metabolite(s) verified positive, and sign and date
the verification statement.
* * * * *
0
9. In Sec. 40.163:
0
a. Paragraph (c)(8) is amended by removing ``and''.
0
b. Paragraph (c)(9) is amended by removing the period at the end and
adding ``; and'' in its place.
0
c. Paragraph (c)(10) is added.
The addition reads as follows:
[[Page 59108]]
Sec. 40.163 How does the MRO report drug test results?
* * * * *
(c) * * *
(10) The DOT Agency, if noted on the CCF.
* * * * *
0
10. In Sec. 40.187, paragraph (f) is revised to read as follows:
Sec. 40.187 What does the MRO do with split specimen laboratory
results?
* * * * *
(f) For all split specimen results, as the MRO you must in Step 7
of Copy 2 of the CCF:
(1) Report split specimen test results by checking the
``Reconfirmed'' box and/or the ``Failed to Reconfirm'' box, or the
``Test Cancelled'' box, as appropriate.
(2), Enter your name, sign, and date.
(3) Send a legible copy of Copy 2 of the CCF (or a signed and dated
letter, see Sec. 40.163) to the employer and keep a copy for your
records. Transmit the document as provided in Sec. 40.167.
0
11. In Sec. 40.191, paragraph (d)(2) is revised, to read as follows:
Sec. 40.191 What is a refusal to take a DOT drug test, and what are
the consequences?
* * * * *
(d) * * *
(2) As the MRO, you must note the refusal by checking the ``Refusal
to Test'' box in Step 6 on Copy 2 of the CCF, checking whether the
specimen was adulterated or substituted and, if adulterated, noting the
adulterant/reason. If there was another reason for the refusal, check
``Other'' in Step 6 on Copy 2 of the CCF, and note the reason next to
the ``Other'' box and on the ``Remarks'' lines, as needed. You must
then sign and date the CCF.
* * * * *
0
12. In Sec. 40.193, paragraph (d)(2)(i) is revised, to read as
follows:
Sec. 40.193 What happens when an employee does not provide a
sufficient amount of urine for a drug test?
* * * * *
(d) * * *
(2) * * *
(i) Check the ``Refusal to Test'' box and ``Other'' box in Step 6
on Copy 2 of the CCF and note the reason next to the ``Other'' box and
on the ``Remarks'' lines, as needed.
* * * * *
0
13. In Sec. 40.203, paragraphs (d)(2) and (d)(3) are revised, to read
as follows:
Sec. 40.203 What problems cause a drug test to be cancelled unless
they are corrected?
* * * * *
(d) * * *
(2) The certifying scientist's signature is omitted on Copy 1 of
the CCF for a positive, adulterated, substituted, or invalid test
result.
(3) The collector uses a non-Federal form or an expired CCF for the
test. This flaw may be corrected through the procedure set forth in
Sec. 40.205(b)(2), provided that the collection testing process has
been conducted in accordance with the procedures of this part in an
HHS-certified laboratory. During the period of October 1, 2010-
September 30, 2011, you are not required to cancel a test because of
the use of an expired CCF. Beginning October 1, 2011, if the problem is
not corrected, you must cancel the test.
0
14. In Sec. 40.209, paragraphs (b)(1) and (b)(9) are revised, to read
as follows:
Sec. 40.209 What procedural problems do not result in the
cancellation of a test and do not require corrective action?
* * * * *
(b) * * *
(1) A minor administrative mistake (e.g., the omission of the
employee's middle initial, a transposition of numbers in the employee's
social security number, the omission of the DOT Agency in Step 1-D of
the CCF.)
* * * * *
(9) Personal identifying information is inadvertently contained on
the CCF (e.g., the employee signs his or her name on Copy 1); or
* * * * *
0
15. In Sec. 40.355, paragraph (l) is revised, to read as follows:
Sec. 40.355 What limitations apply to the activities of service
agents?
* * * * *
(l) In transmitting documents to laboratories, you must ensure that
you send to the laboratory that conducts testing only Copy 1 of the
CCF. You must not transmit other copies of the CCF or any ATFs to the
laboratory.
* * * * *
[FR Doc. 2010-24038 Filed 9-24-10; 8:45 am]
BILLING CODE 4910-9X-P