Specifications include, but are not limited to: 3.1. Work with providers and/or accredited laboratories to perform the services under this Contract; 3.2. Collect SARS-CoV-2 specimens, using appropriate Personal Protection Equipment (PPE) for the specimen type, and Federal Food and Drug Administration (FDA) approved collection kits, including but not limited to nasopharyngeal (NP) swab, nasal swab, nasal wash, saliva, or blood; 3.3. Conduct SARS-CoV-2 testing under an approved FDA Emergecny Use Authorization (EUA) or FDA approval; 3.4. Obtain Clinical Laboratory Improvement Amendment (CLIA) waiver as needed; 3.5. Provide appropriate PPE when screening for symptoms and fever for COVID-19, prior to deployment, for Contractor staff when collecting specimens; 3.6. Collect an ADHS or agency consent form from all participating individuals (will be provided after award); 3.7. Provide standing orders for testing; 3.8. Complete a Google form or other type of documentation designated by ADHS for each location upon completion of each round of specimens collected at each location (will be provided after award); 3.9. Maintain confidentiality of individuals, agencies, and facilities whom specimens were collected under this Contract, regardless of media knowledge; and 3.10. Coordinate and receive approval from ADHS on any press releases, interviews, advertising, or social media related to the testing of these facilities.
