FDA Authorizes First COVID-19 Test for Home Collection Using Saliva
FDA COVID-19 EUA
On May 7, 2020, the US FDA authorized the first COVID-19 test for home collection using saliva. Importantly, the Emergency Use Authorization (EUA) is specifically for the Rutgers Clinical Genomics Laboratory TaqPath SARS-CoV-2 Assay when used with the Spectrum Solutions LLC SDNA-1000 Saliva Collection Device. A healthcare provider must determine the test to be appropriate and the specimen must still be sent to a laboratory for processing and test reporting.
CMS Interim Final Rule: Summary of Key Telehealth Provisions
CMS Interim Final Rule (Part 2)
On April 30, 2020, the Centers for Medicare and Medicaid Services issued an updated interim final rule that further expands Medicare coverage for telehealth. ATA has worked closely with members to advocate for these key policy changes and applauds CMS for continuing to support the rapid expansion of telehealth.
HRSA Launches New CARES Act Fund to Cover COVID-19 Testing and Treatment
Provider Reimbursement of Uninsured Testing and Treatment
On April 27, 2020, the Health and Human Services, Health Resources & Services Administration (HRSA) launched a new CARES-mandated program to reimburse health care providers for COVID-19 related testing and treatment. The HRSA application portal will begin accepting patient information and claims for payment starting May 6.
FDA Authorizes First COVID-19 Test for Home Collection
FDA COVID-19 EUA
On April 20, 2020, the US FDA authorized the first COVID-19 test for home collection of specimens. Importantly, the Emergency Use Authorization (EUA) is specifically for the home specimen collection method for the LabCorp COVID-19 RT-PCR Test. The specimen must still be sent to a laboratory for processing and test reporting.
FCC COVID-19 Telehealth Program Application Guidance
Guidance on Applying for FCC COVID-19 Telehealth Funding
As part of the CARES Act, the FCC launched the $200 million COVID-19 Telehealth Program to support health care providers in expanding telehealth and remote patient monitoring technology to patients. The FCC’s Wireline Competition Bureau will begin accepting applications for the COVID-19 Telehealth Program beginning Monday, April 13, 2020 at 12:00 PM ET at www.fcc.gov/covid19telehealth
FCC COVID-19 Telehealth Program & Connected Care Pilot Program
FAQs for ATA Members
The FCC has launched two funding programs to support health care providers in expanding telehealth and virtual care to patients. The April 2 FCC Report and Order establishes two distinct programs – the COVID-19 Telehealth Program and the Connected Care Pilot Program.
CMS Announces New COVID-19 Telehealth Flexibilities
POLICY UPDATE - 3.31.20
CARES Act Summary (HR 748) - Key Telehealth Provisions
Act Now: ATA Urges MA Plan Members to Apply for CMS’ Value-Based Insurance Design (VBID) Mode
Section 3021 of the Affordable Care Act
In 2018, Congress and CMS recognized our calls to action and provided our industry with a variety of new and unique opportunities to demonstrate the value of telehealth. Perhaps the biggest opportunity created by federal policy changes lies in the Medicare Advantage (MA) program. CMS has allowed three things for the Medicare Advantage population in the coming plan years: 1) the ability to include telehealth in the base bid rather than as a supplemental benefit, 2) the ability to use telehealth providers to meet MA network adequacy standards, and 3) the ability to apply differential cost sharing for “high value providers” (meaning that plans could choose to charge beneficiaries $0 copays for telehealth providers).