Laboratory Testing Sites Clause Samples
The 'Laboratory Testing Sites' clause defines the specific locations where laboratory testing activities must be conducted under the agreement. It typically outlines whether testing is restricted to certain approved facilities, such as accredited laboratories or those meeting regulatory standards, and may require prior written approval for the use of additional or alternative sites. This clause ensures that all testing is performed in controlled, compliant environments, thereby maintaining data integrity, regulatory compliance, and the reliability of test results.
Laboratory Testing Sites. The following provisions shall apply if Provider is a laboratory testing site. Provider shall have either a Clinical Laboratory Improvement Amendments (CLIA) certificate or waiver of a certificate of registration, along with a CLIA identification number. Provider understands that Company will maintain a comprehensive network of independent and other laboratories that ensures laboratories are accessible to all Enrollees. Any Provider performing laboratory tests is required to be certified under CLIA. OHCA will continue to update the Provider file with CLIA information, which Provider acknowledges will make laboratory certification information available to Company on the Medicaid Provider file. (State Contract §1.14.1.3.3)
Laboratory Testing Sites. The following provisions shall apply if Provider is a laboratory testing site. Provider shall have either a Clinical Laboratory Improvement Amendments (CLIA) certificate or waiver of a certificate of registration, along with a CLIA identification number. Provider understands that Company will maintain a comprehensive network of independent and other laboratories that ensures laboratories are accessible to all Covered Persons. Any Provider performing laboratory tests is required to be certified under CLIA. OHCA will continue to update the provider file with CLIA information, which Provider acknowledges will make laboratory certification information available to Company on the Medicaid provider file. (Model Contract 1.12.2.4.3) SCHEDULE B REGULATORY REQUIREMENTS This Schedule sets forth the provisions that are required by State or federal law to be included in the Agreement with respect to the Medicaid Product. Any additional Regulatory Requirements that may apply to the Coverage Agreements or Covered Persons enrolled in or covered by this Product may be set forth in the Provider Manual or another Attachment. To the extent that a Coverage Agreement, or a Covered Person, is subject to the law cited in the parenthetical at the end of a provision on this Schedule B, such provision will apply to the rendering of Covered Services to a Covered Person with such Coverage Agreement, or to such Covered Person, as applicable.
Laboratory Testing Sites. In accordance with the terms of the HealthChoices Waiver, all laboratory testing sites providing services pursuant to this Contract shall have either a Clinical Laboratory Improvement Act (“CLIA”) certificate of waiver or a certificate of registration along with a CLIA identification number. Those laboratories with certificates of waiver will provide only the eight types of tests permitted under the terms of the HealthChoices Waiver. Laboratories with certificates of registration may perform a full range of laboratory tests.