ASBM was an exhibitor during the 52nd Annual meeting of the Drug Information Association (DIA) held June 26th-30th in Philadelphia.
ASBM members and staff discussed biosimilars policy with attendees, including the need for the FDA to maintain high standards for safety and efficacy when approving biosimilars.
More than 65 attendees, including clinical researchers, physicians, pharmacists, patients, and regulators, filled out “Names Matter” postcards urging the FDA to adopt meaningful, memorable suffixes in future biosimilar approvals (as it did in its first approval) rather than random suffixes (as it did in its second).