Diabetes Technologies, Inc.

 

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DTI Laboratories, Inc.

888.872.2443

 

DTI Laboratories, Inc. (DTIL), is a CLIA/CMS certified reference laboratory. DTIL is a Medicare Part B participating provider, performing HbA1c and general chemistry lab procedures. We are a College of American Pathologist (CAP) participating laboratory for glycohemoglobin proficiency testing. DTIL employs NGSP/IFCC certified testing methods.

Scope of service; We currently perform/support A1c analysis for Diabetes Screening, Clinical/Diagnostic monitoring, clinical research for universities, governmental agencies, pharmaceutical companies, and clinical study centers.  Our capillary collection method has been used in over 20 diabetes/cancer clinical trials/studies. we currently support 14 separate University studies. In addition, we support many HMO's and insurance companies for diabetes and kidney outcomes studies and HEDIS markers.

DTIL specializes in human, primate and mouse A1c analysis.

Medical Director: Fred H. Fritzsche, Jr. M.D. Board of Medical Examiners

CLIA#: 11D1006555

Georgia Department of Human Services License: 136-006

Medicare Identification #: 69WBDMF

DTI Labs has been serving the clinical/diagnostic community since 2002.

Procedures:

Hemoglobin A1c

Variant hemoglobin screening

Microalbumin testing

Anemia testing

Lipid Panel

Lead testing

Drug Screening-

    Pre-employment

    Insurance screening

HPLC-ion (IE) exchange A1c analysis- perform variant hemoglobin screening

(ideal for screening out subject with hemoglobinopathies for clinical trial studies)

HPLC-boronate affinity (BA) A1c analysis- perform interference-free A1c analysis

HPLC Multi-method analysis: perform HPLC-IE/BA analysis as directed. Provide information on variants as well as reporting an A1c analysis free of interferences.

A1c capillary analysis including sample collection kits available.  To-date these capillary collection kits (5 ul) sample requirement can be drawn from a finger or direct from a test tube.

Samples are packaged in 1 ml liquid EDTA vials and are stable for 30 days un-refrigerated after sample collection.  The kits are FDA approved and carry a Certificate of Compliance with each shipment.  Samples can be numbered for ease of tracking and lab reporting.

To date over 350,000 samples have been analyzed using this method involving over 2,500 clinical sites. Large lots are available for long-term studies. Results can be transmitted in excel format in PDF format.

Please contact us at 888.872.2443 to request a quotation or to learn more about our laboratory.