What does 2301 mean?
2301 means FDA form for transmittal of periodic reports and promotional material for new animal drugs
What is the abbreviation for FDA form for transmittal of periodic reports and promotional material for new animal drugs?
FDA form for transmittal of periodic reports and promotional material for new animal drugs can be abbreviated as 2301
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Most popular questions people look for before coming to this page
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What does 2301 stand for? 2301 stands for "FDA form for transmittal of periodic reports and promotional material for new animal drugs". |
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How to abbreviate "FDA form for transmittal of periodic reports and promotional material for new animal drugs"? "FDA form for transmittal of periodic reports and promotional material for new animal drugs" can be abbreviated as 2301. |
| Q: A: |
What is the meaning of 2301 abbreviation? The meaning of 2301 abbreviation is "FDA form for transmittal of periodic reports and promotional material for new animal drugs". |
| Q: A: |
What is 2301 abbreviation? One of the definitions of 2301 is "FDA form for transmittal of periodic reports and promotional material for new animal drugs". |
| Q: A: |
What does 2301 mean? 2301 as abbreviation means "FDA form for transmittal of periodic reports and promotional material for new animal drugs". |
| Q: A: |
What is shorthand of FDA form for transmittal of periodic reports and promotional material for new animal drugs? The most common shorthand of "FDA form for transmittal of periodic reports and promotional material for new animal drugs" is 2301. |
Abbreviations or Slang with similar meaning
- JCRI - Journal of Clinical Reports and Images
- EUROFLAX - New integrated approach for the optimisation ofEuropean Flax products through the engineering of the process and material
- INAD - Investigation of New Animal Drugs
- TMRWA - The Majority of these Reports and Warnings Appear
- 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
- 348 - FDA form for sponsored travel
- 3500 - FDA form for voluntary reporting of adverse events
- 3500A - FDA form for mandatory reporting of adverse events
- 356V - FDA form for new animal drug appication
- 482 - FDA form for notice of inspection
- 483 - FDA form used as a written notice of deficiencies found in inspections
- FD-1932 - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory
- FD-1932 - FDA form, 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-2301 - FDA form, 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
- FD-483 - FDA form, Written Notice of Deficiencies Found in Inspections