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.
|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|