FORM 3500A means Mandatory Reporting of Adverse Events in FDA
Similar to FORM 3500A
ADA - Americans with Disabilities Act of 1990ADAA - Animal Drug Availability Act of 1996
ADaM - Analysis Dataset Model
ADAMHA - Alcohol, Drug Abuse, and Mental Health Administration now SAMHSA
ADCOM - advisory committee
ADE - Adverse Drug Event
ADE/ADER - Adverse Drug Experience/Adverse Drug Experience Report
View all in FDA