What does 3500 mean?
3500 means FDA form for voluntary reporting of adverse events
What is the abbreviation for FDA form for voluntary reporting of adverse events?
FDA form for voluntary reporting of adverse events can be abbreviated as 3500
|
|
Most popular questions people look for before coming to this page
| Q: A: |
What does 3500 stand for? 3500 stands for "FDA form for voluntary reporting of adverse events". |
| Q: A: |
How to abbreviate "FDA form for voluntary reporting of adverse events"? "FDA form for voluntary reporting of adverse events" can be abbreviated as 3500. |
| Q: A: |
What is the meaning of 3500 abbreviation? The meaning of 3500 abbreviation is "FDA form for voluntary reporting of adverse events". |
| Q: A: |
What is 3500 abbreviation? One of the definitions of 3500 is "FDA form for voluntary reporting of adverse events". |
| Q: A: |
What does 3500 mean? 3500 as abbreviation means "FDA form for voluntary reporting of adverse events". |
| Q: A: |
What is shorthand of FDA form for voluntary reporting of adverse events? The most common shorthand of "FDA form for voluntary reporting of adverse events" is 3500. |
Abbreviations or Slang with similar meaning
- DAERI - Database of Adverse Events Related to the Internet
- AVSSA - Association for Voluntary Sterilisation of SA
- VRGGP - Voluntary Reporting of Greenhouse Gases Program
- ICSPE - International Centre for the Study of Planned Events
- 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
- 3500A - FDA form for mandatory 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