Current List of HHS-Certified Laboratories and Instrumented Initial Testing Facilities Which Meet Minimum Standards To Engage in Urine Drug Testing for Federal Agencies

Published date01 October 2019
Record Number2019-21176
SectionNotices
CourtSubstance Abuse And Mental Health Services Administration
Federal Register, Volume 84 Issue 190 (Tuesday, October 1, 2019)
[Federal Register Volume 84, Number 190 (Tuesday, October 1, 2019)]
                [Notices]
                [Pages 52117-52118]
                From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
                [FR Doc No: 2019-21176]
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                DEPARTMENT OF HEALTH AND HUMAN SERVICES
                Substance Abuse and Mental Health Services Administration
                Current List of HHS-Certified Laboratories and Instrumented
                Initial Testing Facilities Which Meet Minimum Standards To Engage in
                Urine Drug Testing for Federal Agencies
                AGENCY: Substance Abuse and Mental Health Services Administration, HHS.
                ACTION: Notice.
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                SUMMARY: The Department of Health and Human Services (HHS) notifies
                federal agencies of the laboratories and Instrumented Initial Testing
                Facilities (IITF) currently certified to meet the standards of the
                Mandatory Guidelines for Federal Workplace Drug Testing Programs
                (Mandatory Guidelines). A notice listing all currently HHS-certified
                laboratories and IITFs is published in the Federal Register during the
                first week of each month. If any laboratory or IITF certification is
                suspended or revoked, the laboratory or IITF will be omitted from
                subsequent lists until such time as it is restored to full
                certification under the Mandatory Guidelines. If any laboratory or IITF
                has withdrawn from the HHS National Laboratory Certification Program
                (NLCP) during the past month, it will be listed at the end and will be
                omitted from the monthly listing thereafter. This notice is also
                available on the internet at http://www.samhsa.gov/workplace.
                FOR FURTHER INFORMATION CONTACT: Charles LoDico, Division of Workplace
                Programs, SAMHSA/CSAP, 5600 Fishers Lane, Room 16N02C, Rockville,
                Maryland 20857; 240-276-2600 (voice).
                SUPPLEMENTARY INFORMATION: The Department of Health and Human Services
                (HHS) notifies federal agencies of the laboratories and Instrumented
                Initial Testing Facilities (IITF) currently certified to meet the
                standards of the Mandatory Guidelines for Federal Workplace Drug
                Testing Programs (Mandatory Guidelines). The Mandatory Guidelines were
                first published in the Federal Register on April 11, 1988 (53 FR
                11970), and subsequently revised in the Federal Register on June 9,
                1994 (59 FR 29908); September 30, 1997 (62 FR 51118); April 13, 2004
                (69 FR 19644); November 25, 2008 (73 FR 71858); December 10, 2008 (73
                FR 75122); April 30, 2010 (75 FR 22809); and on January 23, 2017 (82 FR
                7920).
                 The Mandatory Guidelines were initially developed in accordance
                with Executive Order 12564 and section 503 of Public Law 100-71. The
                ``Mandatory Guidelines for Federal Workplace Drug Testing Programs,''
                as amended in the revisions listed above, requires strict standards
                that laboratories and IITFs must meet in order to conduct drug and
                specimen validity tests on urine specimens for federal agencies.
                 To become certified, an applicant laboratory or IITF must undergo
                three rounds of performance testing plus an on-site inspection. To
                maintain that certification, a laboratory or IITF must participate in a
                quarterly performance testing program plus undergo periodic, on-site
                inspections.
                 Laboratories and IITFs in the applicant stage of certification are
                not to be considered as meeting the minimum requirements described in
                the HHS Mandatory Guidelines. A HHS-certified laboratory or IITF must
                have its letter of certification from HHS/SAMHSA (formerly: HHS/NIDA),
                which attests that it has met minimum standards.
                 In accordance with the Mandatory Guidelines dated January 23, 2017
                (82 FR 7920), the following HHS-certified laboratories and IITFs meet
                the minimum standards to conduct drug and specimen validity tests on
                urine specimens:
                HHS-Certified Instrumented Initial Testing Facilities
                Dynacare, 6628 50th Street NW, Edmonton, AB Canada T6B 2N7, 780-784-
                1190 (Formerly: Gamma-Dynacare Medical Laboratories).
                HHS-Certified Laboratories
                ACM Medical Laboratory, Inc., 160 Elmgrove Park, Rochester, NY 14624,
                844-486-9226.
                Alere Toxicology Services, 1111 Newton St., Gretna, LA 70053, 504-361-
                8989/800-433-3823 (Formerly: Kroll Laboratory Specialists, Inc.,
                Laboratory Specialists, Inc.).
                Alere Toxicology Services, 450 South lake Blvd., Richmond, VA 23236,
                804-378-9130 (Formerly: Kroll Laboratory Specialists, Inc., Scientific
                Testing Laboratories, Inc.; Kroll Scientific Testing Laboratories,
                Inc.).
                Baptist Medical Center-Toxicology Laboratory, 11401 I-30, Little Rock,
                AR 72209-7056, 501-202-2783 (Formerly: Forensic Toxicology Laboratory
                Baptist Medical Center).
                Clinical Reference Laboratory, Inc., 8433 Quiver Road, Leone, KS 66215-
                2802, 800-445-6917.
                Cordant Health Solutions, 2617 East L Street, Tacoma, WA 98421, 800-
                442-0438 (Formerly: STERLING Reference Laboratories).
                Desert Ox, LLC, 10221 North 32nd Street Suite J, Phoenix, AZ 85028,
                602-457-5411.
                Drug, Scan, Inc., 200 Precision Road, Suite 200, Horsham, PA 19044,
                800-235-4890.
                Dynacare,*245 Pall Mall Street, London, ONT, Canada N6A 1P4, 519-679-
                1630 (Formerly: Gamma-Dynacare Medical Laboratories).
                ElSohly Laboratories, Inc., 5 Industrial Park Drive, Oxford, MS 38655,
                662-236-2609.
                Laboratory Corporation of America Holdings, 7207 N. Gessner Road,
                Houston, TX 77040, 713-856-8288/800-800-2387.
                Laboratory Corporation of America Holdings, 69 First Ave., Raritan, NJ
                08869, 908-526-2400/800-437-4986 (Formerly: Roche Biomedical
                Laboratories, Inc.).
                Laboratory Corporation of America Holdings, 1904 TW Alexander Drive,
                Research Triangle Park, NC 27709, 919-572-6900/800-833-3984 (Formerly:
                LabCorp Occupational Testing Services, Inc., CompuChem Laboratories,
                Inc.; CompuChem Laboratories, Inc., A Subsidiary of Roche Biomedical
                Laboratory; Roche CompuChem Laboratories, Inc., A Member of the Roche
                Group).
                 Laboratory Corporation of America Holdings, 1120 Main Street,
                Southaven, MS 38671, 866-827-8042/800-233-6339 (Formerly: LabCorp
                Occupational Testing Services, Inc.; MedExpress/National Laboratory
                Center).
                LabOne, Inc. d/b/a Quest Diagnostics, 10101 Renner Blvd., Lenexa, KS
                66219, 913-888-3927/800-873-8845 (Formerly: Quest Diagnostics
                Incorporated; LabOne, Inc.; Center for Laboratory Services, a Division
                of LabOne, Inc.).
                [[Page 52118]]
                Legacy Laboratory Services--MetroLab, 1225 NE 2nd Ave., Portland, OR
                97232, 503-413-5295/800-950-5295.
                MedTox Laboratories, Inc., 402 W. County Road D, St. Paul, MN 55112,
                651-636-7466/800-832-3244.
                Minneapolis Veterans Affairs Medical Center, Forensic Toxicology
                Laboratory, 1 Veterans Drive, Minneapolis, MN 55417, 612-725-2088,
                Testing for Veterans Affairs (VA) Employees Only.
                Pacific Toxicology Laboratories, 9348 DeSoto Ave., Chatsworth, CA
                91311, 800-328-6942 (Formerly: Centinela Hospital Airport Toxicology
                Laboratory).
                Pathology Associates Medical Laboratories, 110 West Cliff Dr., Spokane,
                WA 99204, 509-755-8991/800-541-7891x7.
                Phamatech, Inc., 15175 Innovation Drive, San Diego, CA 92128, 888-635-
                5840.
                Quest Diagnostics Incorporated, 1777 Montreal Circle, Tucker, GA 30084,
                800-729-6432 (Formerly: SmithKline Beecham Clinical Laboratories;
                SmithKline Bio-Science Laboratories).
                Quest Diagnostics Incorporated, 400 Egypt Road, Norristown, PA 19403,
                610-631-4600/877-642-2216 (Formerly: SmithKline Beecham Clinical
                Laboratories; SmithKline Bio-Science Laboratories).
                Redwood Toxicology Laboratory, 3700 Westwind Blvd., Santa Rosa, CA
                95403, 800-255-2159.
                US Army Forensic Toxicology Drug Testing Laboratory, 2490 Wilson St.,
                Fort George G. Meade, MD 20755-5235, 301-677-7085, Testing for
                Department of Defense (DoD) Employees Only.
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                 * The Standards Council of Canada (SCC) voted to end its
                Laboratory Accreditation Program for Substance Abuse (LAPSA)
                effective May 12, 1998. Laboratories certified through that program
                were accredited to conduct forensic urine drug testing as required
                by U.S. Department of Transportation (DOT) regulations. As of that
                date, the certification of those accredited Canadian laboratories
                will continue under DOT authority. The responsibility for conducting
                quarterly performance testing plus periodic on-site inspections of
                those LAPSA-accredited laboratories was transferred to the U.S. HHS,
                with the HHS' NLCP contractor continuing to have an active role in
                the performance testing and laboratory inspection processes. Other
                Canadian laboratories wishing to be considered for the NLCP may
                apply directly to the NLCP contractor just as U.S. laboratories do.
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                 Upon finding a Canadian laboratory to be qualified, HHS will
                recommend that DOT certify the laboratory (Federal Register, July 16,
                1996) as meeting the minimum standards of the Mandatory Guidelines
                published in the Federal Register on January 23, 2017 (82 FR 7920).
                After receiving DOT certification, the laboratory will be included in
                the monthly list of HHS-certified laboratories and participate in the
                NLCP certification maintenance program.
                Charles P. LoDico,
                Chemist.
                [FR Doc. 2019-21176 Filed 9-30-19; 8:45 am]
                BILLING CODE 4162-20-P
                

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