What does CAERST (CFSAN) mean?
CAERST (CFSAN) means CFSAN Adverse Event Reporting System Team
What is the abbreviation for CFSAN Adverse Event Reporting System Team?
CFSAN Adverse Event Reporting System Team can be abbreviated as CAERST (CFSAN)
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Most popular questions people look for before coming to this page
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What does CAERST (CFSAN) stand for? CAERST (CFSAN) stands for "CFSAN Adverse Event Reporting System Team". |
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How to abbreviate "CFSAN Adverse Event Reporting System Team"? "CFSAN Adverse Event Reporting System Team" can be abbreviated as CAERST (CFSAN). |
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What is the meaning of CAERST (CFSAN) abbreviation? The meaning of CAERST (CFSAN) abbreviation is "CFSAN Adverse Event Reporting System Team". |
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What is CAERST (CFSAN) abbreviation? One of the definitions of CAERST (CFSAN) is "CFSAN Adverse Event Reporting System Team". |
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What does CAERST (CFSAN) mean? CAERST (CFSAN) as abbreviation means "CFSAN Adverse Event Reporting System Team". |
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What is shorthand of CFSAN Adverse Event Reporting System Team? The most common shorthand of "CFSAN Adverse Event Reporting System Team" is CAERST (CFSAN). |
Abbreviations or Slang with similar meaning
- SN/AEMS - Special Nutritionals Adverse Event Monitoring System
- VAERS - Vaccine Adverse Event Reporting System
- AER - Adverse Event Reporting
- CAERS - CFSAN (Center for Food Safety and Applied Nutrition) Adverse Event Reporting System
- ADRS - Adverse Drug Reporting System
- AEMS - Adverse Event Monitoring System
- AERC - Adverse Event Reporting Consultants
- AIRS - Adverse Incident Reporting System
- AORS - Adverse Occurrence Reporting System
- ARRS - Adverse Reactions Reporting System
- CAER - Computerized Adverse Event Reporting
- aero - Adverse Event Reporting Ontology
- ers - Event Reporting System
- saer - Serious Adverse Event Reporting
- VAERS - Vaccine Adverse Event Report System
- AERS - Adverse Event Reporting System (Food & Drug Administration)
- CAERS - CFSAN Adverse Event Reporting System
- FAEMS - Foods Adverse Event Monitoring System
- FAERS - FDA Adverse Event Reporting System
- MEDWATCH - FDA Safety Information and Adverse Event Reporting Program