What does 3500A mean Governmental FDA ?

This is a page where explained definition of 3500A - acronym, abbreviation or shorthand form.
On this page you can see detailed information about 3500A as it is used in Governmental- FDA sector.


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3500A in Governmental FDA means:

FDA form for mandatory reporting of adverse events

3500A in Governmental FDA stands for: FDA form for mandatory reporting of adverse events, but what about the same or alike Acronyms?

Maybe you are also interested other acronyms like 3500A which are used with different definition and different situations? Here they are, below.

Similar acronyms

Short form   Meaning Category Second Category
3500A Means FDA form for mandatory reporting of adverse events Governmental FDA
3500 Means FDA form for voluntary reporting of adverse events Governmental FDA
FORM 3500A Means Mandatory Reporting of Adverse Events Governmental FDA
FD-1932 Means FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory Governmental US Government
FD-1932 Means FDA form, Veterinary Adverse Drug Reaction, lack of effectiveness, product defect report - Mandatory Governmental FDA
FAERS Means FDA Adverse Event Reporting System Governmental FDA
MEDWATCH Means FDA Safety Information and Adverse Event Reporting Program Governmental FDA
FD-1932a Means FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report - voluntary Governmental FDA
1932a Means FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--voluntary Governmental FDA
FD-1932a Means FDA form, Veterinary Adverse Drug Reaction, lack of effectiveness, product defect report - Voluntary Governmental FDA
FORM 3500 Means Voluntary Reporting of Adverse Events Governmental FDA
VAERS Means Vaccine Adverse Events Reporting System Medical British Medicine
FORM 1932 Means Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report - Mandatory Governmental FDA
482 Means FDA form for notice of inspection Governmental FDA
ADE Means Adverse Drug Events Medical Drugs
AEFI Means Adverse Events Following Immunisation Miscellaneous Unclassified
OAE Means Ontology of Adverse Events Miscellaneous Unclassified
AEFI Means Adverse Events Following Immunization Miscellaneous Unclassified
AEP Means Adverse Events Profile Medical Hospitals
FD-356V Means FDA form, New Animal Drug Application Governmental FDA
356V Means FDA form for new animal drug appication Governmental FDA
FD-356V Means FDA form for new animal drug application Governmental US Government
NSAE Means Nurse Sensitive Adverse Events Medical Nursing
TEAE Means treatment emergent adverse events Miscellaneous Unclassified
MACE Means Major Adverse Cardiac Events Medical Cardiology