Our global life sciences company brings diagnostic testing & drug development together.


The primary focus of Labcorp Corporate Solutions is to provide consistently good service. For customer convenience, the following online forms are designed to direct your inquiries appropriately.

Request Labcorp Corporate Solutions sales assistance
Telephone: 800-343-8974 (voicemail)
For occupational testing set up or for additional information on our services, contact a Labcorp Corporate Solutions sales representative.

Order drug testing supplies
Telephone: 800-833-3984
Allows Labcorp clients to order drug and alcohol testing supplies (Labcorp account number required).

Request customer service
Telephone: 800-833-3984
Allows Labcorp clients to submit request for customer service assistance to Labcorp’s Occupational Testing Services customer operations department.

Web Tools FAQs

  • What is Donor Registration?

    The LabCorp Corporate Solutions Web Tools Donor Registration feature enables the user to create a drug screen test order record that may be retrieved by the specimen collector in Web COC. Donor Registration assists employers in assuring that company drug testing deadlines are met, since the user may set a donor registration expiration date. Donor Registration enables the user to elect to receive email notification of each specimen collection completion or donor no-show. 

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  • What is the process for removing inactive users?

    Complete the applicable LabCorp Corporate Solutions user registration form. Indicate on the user registration form that you are removing a user’s access. Submit completed and signed user registration forms to LabCorp occupational testing services by faxing to 919-481-5444 or emailing [email protected]

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Toxicology FAQs

  • Why are screening and confirmation cut-off levels different?

    Simply stated, screening and confirmation testing are performed using different testing methodologies that have different specificity and sensitivity. The immunoassay tests used to perform initial drug screening are designed to detect a wide range of chemically similar compounds that react with the antibodies which are at the core of the chemistry making up the tests. The combined cross-reactivity of compounds in the drug class may elicit a positive response, even though an individual metabolite may be present below the initial test cutoff. When performing confirmation testing by GC/MS or LC/MS/MS, one or more specific metabolites can be identified, quantified and reported using the applicable confirmation cutoff for a positive test result. 

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  • To what does ng/mL refer?

    Nanograms per milliliter, abbreviated ng/mL, is the unit of measure most commonly used to express drug testing cut-off levels and quantitative test results in urine and oral fluid. A nanogram is 10-9 grams. 

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  • What is specimen validity testing?

    Specimen validity testing (SVT) is performed on a urine drug screen specimen to detect substitution, adulteration, or dilution. See the Drugs of Abuse Reference Guide for additional information on SVT. Use of a Medical Review Officer is recommended to evaluate out of range SVT results.

    • Substitution - Submission of a specimen that is not characteristic of human urine. Typically, this may be water or water with salt in it and is identified by extreme creatinine and specific gravity results.
    • Adulteration - Adding a substance to a specimen after it has been collected. The product added is designed to mask the presence of, or chemically destroy, the drug or drug metabolite that the specimen may contain. An adulterant product may be added with the intention of adversely affecting the testing reagents.
    • Dilution - Result of ingestion of large amounts of water typically just before urine donation or as a result of physiological conditions. If drug/metabolites are diluted to a concentration below the initial test cutoff, a dilute urine may result in a false negative.

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