Robert Califf, commissioner of the US Food and Drug Administration (FDA), said the agency is looking at new ways to assess bioequivalence and increase its early interactions with industry to promote more first-cycle approvals of complex generics at a 20 September webinar sponsored by FDA’s Small Business and Industry Assistance (SBIA) program.
privacy policy | terms of use | contact us | advertise | pharma jobs | pharma blogs | facebook | twitter
Copyright © 2024,