Laboratory Certification. Licensure. Contractor shall be certified to perform drug testing by the U.S. Department of Health and Human Services (DHHS) under the National Laboratory Certification Program (NLCP). As a laboratory participating in the DOT testing program, you must comply with the requirements of 49 CFR Part 40 Subpart F. You must also comply with all applicable requirements of DHHS in testing DOT specimens, whether or not these requirements are explicitly stated in 49 CFR Part 40 Subpart F. Failure to maintain Certification is cause for termination of this Agreement. The lab shall not subcontract, and shall perform all work with its own personnel and equipment. Contractor shall assure that its facilities comply with applicable provisions of any state licensure and health requirements and local government ordinances and regulations.
Laboratory Certification. If Provider is a laboratory testing site or provides laboratory services to Covered Persons, Provider must maintain a Clinical Laboratory Improvement Amendment (“CLIA”) Certificate of Waiver, Certificate of Accreditation, or a Certificate of Registration along with a CLIA identification number.
Laboratory Certification. Illinois EPA and IDPH will continue to provide an adequate laboratory certification program for all regulated contaminants, at a minimum; to certify commercial laboratories at least once every three years; ensure capacity to analyze at the principal state laboratory or commercial labs all NPDWR parameters that are required to be sampled in the State; and maintain certification for the principal state labs. - Illinois EPA and IDPH Lab Certification Programs will continue to submit annual questionnaires to U.S. EPA Region 5.
Laboratory Certification. The chemical laboratory must be certified by Xxxxx Corning per procedure *. Any change in analytical procedure requires re-certification. If the supplier does not employ a certified chemical laboratory, then he must submit a schedule by which his chemical laboratory will achieve certification. This schedule must be mutually agreed upon by the supplier and Xxxxx Corning.
Laboratory Certification. Contractor’s laboratory performing analyses on City samples must be approved by the Environmental Protection Agency (EPA) for raw water and drinking water analyses and certified by the Michigan Department of Environmental Quality (MDEQ) to perform drinking water analyses for compliance purposes in the state of Michigan. In addition, the Contractor must provide demonstrated competence to perform the specified NPDES test methods required under the City’s NPDES permits. The Contractor is preferably accredited in accordance with the National Environmental Laboratory Accreditation Program (NELAP).
Laboratory Certification. Indiana will continue to provide an adequate laboratory certification program for all regulated contaminants, at a minimum, to certify commercial laboratories at least once every three years; ensuring capacity to analyze at the Principal State Laboratory or commercial laboratories all NPDWR parameters that are required to be sampled in the State; and maintain certification for the Principal State Laboratory. - IDEM is under a Memorandum of Agreement with the IDOH to implement the Laboratory Certification Program and to serve as the Principal State Laboratory. IDOH will certify all laboratories performing analyses for compliance with the SDWA. IDOH is performing procedures established in accordance with the Manual for the Certification of Laboratories for Analyzing Drinking Water. IDOH will continue to submit the annual questionnaires to the Region as requested. - In FY 2021 and FY 2022, Indiana will continue to dedicate PWSS funding for IDEM staff that assist IDOH labs on maintaining the list of certified drinking water labs. IDEM staff maintain the certified lab data in SDWIS/State.
Laboratory Certification. All contractors performing sample analysis must have an Environmental Laboratory Accreditation Program Certificate and shall provide evidence of such certification upon request by the CSP.
Laboratory Certification. A. To ensure that each laboratory used to perform services under this Contract or by Subcontract complies with federal and State law, each location at which any test or examination on materials derived from the human body for the purpose of providing information for the diagnosis, prevention, treatment or assessment of any disease, impairment, or health of a human being is performed shall have in effect:
1. A current, unrevoked or unsuspended certificate, certificate for provider-performed microscopy procedures, certificate of accreditation, certificate of registration or certificate of waiver issued under the requirements of 00 Xxxxxx Xxxxxx Code Section 263a and the regulations adopted thereunder and found at 42 Code of Federal Regulations, Part 493; and, either
a. A current, unrevoked or unsuspended license or registration issued under the requirements of Chapter 3 (commencing with Section 1200) of Division 2 of the California Business and Professions Code and the regulations adopted thereunder; or,
b. Be operated in conformity with Chapter 7 (commencing with Section 1000) of Division 1 of the California Health and Safety Xxxxxx Medical Centers 95-23637 Article III Code and the regulations adopted thereunder.
B. All places used to perform tests or examinations on human biological specimens (materials derived from the human body) are, by definition, "laboratories" under State and federal law.
C. Laboratories may exist, therefore, at Nurses' stations within hospitals, clinics, Skilled Nursing Facilities, operating rooms, surgical centers, rural health clinics, Physician offices, Xxxxxxx Xxxxxxxxxx clinics, mobile labs, health fairs, and city, county or State labs.
D. Any laboratory that does not comply with the appropriate federal and State law is not eligible for participation in, or reimbursement from, the Medicare, Medicaid, or Medi-Cal programs.
