A Final LDT Rule in April!? Will FDA be prepared?
FDA Law Blog
DECEMBER 11, 2023
This is based on FDA’s reported 2018 review of the CLIA database. [2] This is 50% greater than the 2018 numbers relied upon by FDA in its estimates. [3] Unless FDA provides timely responses to pre-submissions, laboratories (and current IVD manufacturers) will not be able to submit applications that address FDA’s expectations.
Let's personalize your content