What does FORM 3500A mean Governmental FDA ?
This is a page where explained definition of FORM 3500A - acronym, abbreviation or shorthand form.
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FORM 3500A in Governmental FDA means:
Mandatory Reporting of Adverse Events
FORM 3500A in Governmental FDA stands for: Mandatory Reporting of Adverse Events, but what about the same or alike Acronyms?
Maybe you are also interested other acronyms like FORM 3500A which are used with different definition and different situations? Here they are, below.
|Short form||Meaning||Category||Second Category|
|FORM 3500A||Means||Mandatory Reporting of Adverse Events||Governmental||FDA|
|3500A||Means||FDA form for mandatory reporting of adverse events||Governmental||FDA|
|FORM 3500||Means||Voluntary Reporting of Adverse Events||Governmental||FDA|
|VAERS||Means||Vaccine Adverse Events Reporting System||Medical||British Medicine|
|3500||Means||FDA form for voluntary reporting of adverse events||Governmental||FDA|
|FORM 1932||Means||Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report - Mandatory||Governmental||FDA|
|AEP||Means||Adverse Events Profile||Medical||Hospitals|
|AEFI||Means||Adverse Events Following Immunisation||Miscellaneous||Unclassified|
|AEFI||Means||Adverse Events Following Immunization||Miscellaneous||Unclassified|
|ADE||Means||Adverse Drug Events||Medical||Drugs|
|OAE||Means||Ontology of Adverse Events||Miscellaneous||Unclassified|
|FD-1932||Means||FDA form, Veterinary Adverse Drug Reaction, lack of effectiveness, product defect report - Mandatory||Governmental||FDA|
|FD-1932||Means||FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory||Governmental||US Government|
|NSAE||Means||Nurse Sensitive Adverse Events||Medical||Nursing|
|NSAE||Means||Nursing Sensitive Adverse Events||Medical||Nursing|
|MACE||Means||Major Adverse Cardiac Events||Medical||Cardiology|
|TEAE||Means||treatment emergent adverse events||Miscellaneous||Unclassified|
|WDAE||Means||Withdrawal Due to Adverse Events||Medical|
|MACCE||Means||Major adverse cardiac and cerebrovascular events||Medical||Cardiology|
|CTCAE||Means||Common Terminology Criteria for Adverse Events||Governmental||FDA|
|MOR||Means||Mandatory Occurrence Reporting||Governmental||Law & Legal|
|CTCAE||Means||common terminology criteria for adverse events (NCI)||Medical|
|MART||Means||Mandatory Abuse Reporting Training||Governmental||Law & Legal|
|MSTR||Means||Mandatory Suspicious Transaction Reporting||Business||Banking|
|MDR||Means||Mandatory Medical Device Reporting||Governmental||US Government|