SQA

FEBRUARY 15, 2023

” The reason: The existing document of the EU GMP Guideline dates back to 2011 and no longer corresponds to the state of the art in various areas or does not consider increasingly important new technologies for the GMP field, according to the EMA. ” The requirements for providers (e.g.,

US Department of Health and Human Services 40

US Department of Health and Human Services FDA COVID-19 World Health 40

Healthcare IT News - Telehealth

MARCH 18, 2022

Out of the $15 billion invested in digital health in 2020 and $29 billion in 2021, on-demand healthcare – including telemedicine streaming video or text-based visits with a healthcare provider – has been the single largest trend, although it is still just the tip of the iceberg with all of the funding activity occurring now.

Medicaid 206

Medicaid Medicaid COVID-19 Telemedicine 206

Drug & Device Law

MAY 19, 2023

The core premise of Bexis’ article is very simple: Once the FDA has said “yes” and approved a particular drug for a particular indication (“intended use”) for sale in the United States, federal preemption precludes any state from saying say “no” and trying to ban that same FDA-approved drug. at *2 (citation omitted).

FDA 111

FDA Medical Personnel Telemedicine Licensing 111