The U.S. Food and Drug Administration (FDA) recently added six new substances to its
The U.S. Food and Drug Administration (FDA) announced on April 24, 2018, that the requirement to submit all new Type III Drug Master File (DMF)
With respect to the PackagingLaw.com article,
Keller and Heckman Partner Mitzi Clark will provide an update on California’s Proposition 65 at the National Association of Printing Ink
The U.S. Food and Drug Administration (FDA) recently added eleven new substances to its
