India  

United States: Regulation Of Digital Health Products By FDA - Foley & Lardner

Mondaq Tuesday, 11 July 2023
Industry insiders can all agree that the U.S. Food & Drug Administration (FDA) regulates the use of medical devices. Most insiders agree that a medical device is any instrument, apparatus...
0
shares
ShareTweetSavePostSend
 

You Might Like


Related videos from verified sources

FDA, Ministry of Truth, warn of health misinformation, urge to consult 'reliable' sources [Video]

FDA, Ministry of Truth, warn of health misinformation, urge to consult 'reliable' sources

The United States Food and Drug Administration (FDA) rightfully warns of misinformation, which they publicly define as false, inaccurate or misleading information. Some opinions disguised as fact are..

Credit: Rumble     Duration: 01:20Published
Juul Seeks US Authorization for New E-Cigarette After 2022 Ban [Video]

Juul Seeks US Authorization for New E-Cigarette After 2022 Ban

Juul Seeks US Authorization , for New E-Cigarette , After 2022 Ban. On July 19, Juul Labs announced it was seeking regulatory authorization for a new e-cigarette to sell in the United States. On..

Credit: Wibbitz Top Stories     Duration: 01:31Published

Related news from verified sources

United States: Episode 26: TLDR: A General Counsel's Perspective On Digital Health (Podcast) - Foley & Lardner

We are excited to announce a special series, TLDR. TLDR is focused on the digital health industry and the lawyers operating inside the companies innovating in...
Mondaq