FDA Law Blog
NOVEMBER 1, 2023
Regulating LDTs: A Long and Winding Road In what might sound to some like protesting too much, the PR invokes FDA’s longstanding assertion that IVDs “manufactured” by laboratories are medical devices and that clinical laboratories that develop tests are acting as manufacturers.
My Green Doctor
MAY 3, 2025
A 2010 research study found that treating two patients per bottle instead of one would decrease plastic waste by approximately 12.69 The product manufacturers and vendors will need to be active partners as well. Eye 24 , 361–363 (2010). tons in the United Kingdom each year. hospital upwards of $240,000 over 5 years. 3 “Each U.S.
CDOCS
APRIL 14, 2021
<br /> <br /> In 2010, I upgraded to the Bluecam and also added the necessary armamentarium to be able to produce e.max restorations in office.& .& We were placing VITA Mark II and Empress restorations on *gasp* second molars.& & What a difference!&
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