A Citizen Petition has been submitted to the Food and Drug Administration (FDA) requesting that the agency issue “final guidance or regulations describing the recommended or required contents of premarket submissions…” In addition to requesting this final guidance, petitioners (NJOY et. al.) are...
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.