What does 3500A mean?
3500A means FDA form for mandatory reporting of adverse events
What is the abbreviation for FDA form for mandatory reporting of adverse events?
FDA form for mandatory reporting of adverse events can be abbreviated as 3500A
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Most popular questions people look for before coming to this page
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What does 3500A stand for? 3500A stands for "FDA form for mandatory reporting of adverse events". |
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How to abbreviate "FDA form for mandatory reporting of adverse events"? "FDA form for mandatory reporting of adverse events" can be abbreviated as 3500A. |
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What is the meaning of 3500A abbreviation? The meaning of 3500A abbreviation is "FDA form for mandatory reporting of adverse events". |
| Q: A: |
What is 3500A abbreviation? One of the definitions of 3500A is "FDA form for mandatory reporting of adverse events". |
| Q: A: |
What does 3500A mean? 3500A as abbreviation means "FDA form for mandatory reporting of adverse events". |
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What is shorthand of FDA form for mandatory reporting of adverse events? The most common shorthand of "FDA form for mandatory reporting of adverse events" is 3500A. |
Abbreviations or Slang with similar meaning
- DAERI - Database of Adverse Events Related to the Internet
- ICSPE - International Centre for the Study of Planned Events
- safer - Spousal Assault Form for the Evaluation of Risk
- BUFR - Binary Universal Form for the Representation (of data)
- SIRE - Society for the Investigation of Recurring Events
- COSTART - Coding Symbols for a Thesaurus of Adverse Reaction Terms-See also MedDRA
- 1932 - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory
- 1932a - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--voluntary
- 2301 - FDA form for transmittal of periodic reports and promotional material for new animal drugs
- 348 - FDA form for sponsored travel
- 3500 - FDA form for voluntary reporting of adverse events
- 356V - FDA form for new animal drug appication
- 482 - FDA form for notice of inspection
- FD-1932 - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory
- FD-1932a - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report - voluntary
- FD-2301 - FDA form for transmittal of periodic reports and promotional material for new animal drugs
- FD-356V - FDA form for new animal drug application
- FD-483 - FDA form 483, written notice of deficiencies found in inspections
- FORM 3500 - Voluntary Reporting of Adverse Events
- FORM 3500A - Mandatory Reporting of Adverse Events