McGraw and Shabbir Review Drug Manufacturing Rules at FDLI Training Event

Shook, Hardy & Bacon Pharmaceutical and Medical Device Associates Stephanie McGraw and Nazish Shabbir explain Current Good Manufacturing Practices and other U.S. Food and Drug Administration drug manufacturing regulations during the Food and Drug Law Institute’s Introduction to Drug Law and Regulation training course slated for April 12-13, 2016, in Washington, D.C.

Their presentation also includes overviews of foreign and domestic inspection processes and definitions of “adulteration” and “misbranding.”