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Point-of-Care diagnostic Tests Direct from Manufacturers

 

 

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~ SHOP PRODUCTS
 
  • Alcohol
      - AlcoScreen
      - BreathScan
      - QED A150

  • Adulteration

  • Cancer Markers

  • Cardiac Markers

  • Chlamydia Test

  • Cholesterol

  • CLIAwaived Drug Tests

  • Dengue Fever

  • Diabetes

  • Drug Test Cards
      - ACON (cards and cups)
      - Buprenorphine
      - CLIAwaived Drug Testing
      - Generic Drug Test Cards
      - iCup - One Step Cup
      - Oxycontin Drug Test
      - Marijuana Drug Test
      - QuikScreen - One Step Cup
      - Rohypnol Test
      - SureStep Drug Test Cards
      - Xanax Test
      - Instant View Test Cards

  • Drug Test Cups
      - EZ Split Drug Test Cup
      - iCup - One Step Cup
      - QuikScreen Drug Test Cup

  • Drug Test (Saliva)

  • Drug Test (Hair)

  • Fecal Occult Blood

  • Flu Test

  • Glucose Testing

  • HIV (AIDS) Testing

  • H Pylori Testing

  • Infectious Disease Test

  • Influenza Testing

  • Ketone Test Strip

  • Malaria Test

  • Mono Test

  • Monthly Specials- Drug Test Kits

  • Monthly Specials- Clinical Tests

  • Nicotine Test

  • Ovulation Test

  • Pregnancy Test

  • RSV Test

  • Strep A Test

  • Syphilis Test

  • Thyroid Testing

  • Tuberculosis Test

  • Urine Test Strips

~ ABOUT US
~ ABOUT CLIA
~ CUSTOMER SERVICE
~ CONTACT
  CORPORATE:
CLIAWaived.com
4332 Corte de la Fonda
San Diego, CA 92130
858-481-5031
SALES:
Toll Free 1-888-882-7739
info@cliawaived.com

 



 

About CLIA

cliawaived.com
4332 Corte De La Fonda
San Diego, CA 92130
Telephone: 858-481-5031, Email: info@cliawaived.com
 




CLIAWaived.com has provided many helpful links below for your review. If you need any help locating or purchasing a CLIA waived device please contact us by email at info@cliawaived.com or call us toll free at 888-882-7739.

Background about CLIA
The Clinical Laboratory Improvement Amendments of 1988 (CLIA) law specified that laboratory requirements be based on the complexity of the test performed and established provisions for categorizing a test as waived.

Tests may be waived from regulatory oversight if they meet certain requirements established by the statute. On February 28, 1992, regulations were published to implement CLIA. In the regulations, waived tests were defined as simple laboratory examinations and procedures that are cleared by the FDA for home use, employ methodologies that are so simple and accurate that mistakes are unlikely and negligible; or pose no reasonable risk of harm to the patient if performed incorrectly. To view a listing of waived tests click one of the links below:
Waived tests
Waived Analytes

Who regulates the CLIA Program?
CMS (Center for Medicare and Medicaid Services) regulates all laboratory testing (except research) performed on humans in the U.S. through the Clinical Laboratory Improvement Amendments (CLIA). In total CLIA covers approximately 175,000 laboratory entities. The Division of Laboratory Services, within the Survey and Certification Group, under CMS has the responsibility for implementing the CLIA Program.

Does my office or company need to apply for a certificate?
CLIA requires that all entities that perform even one test, including a waived test on ..."materials derived from the human body for the purpose of providing information for diagnosis, prevention or treatment of any disease or impairment of, or the assessment of the health of, human beings" to meet certain Federal requirements. If any entity performs tests for these purposes, it is considered under CLIA to be a laboratory and must register with the CLIA program.

How do I apply for a CLIA Certificate?
CLICK HERE (new window will open)

How do I contact my state office?
CLICK HERE (PDF - new window will open)

Where do I mail my renewal fee for CLIA licensure?
Please do not mail check to CLIAwaived,Inc. All checks for CLIA licensure fee's should be made payable to
"CLIA LABORATORY PROGRAM"  and addressed to:

CLIA LABORATORY PROGRAM
P.O. BOX 105422
Atlanta, GA 30348-5422