What does saer mean?
saer means Serious Adverse Event Reporting
This acronym/slang usually belongs to Undefined category.
What is the abbreviation for Serious Adverse Event Reporting?
Serious Adverse Event Reporting can be abbreviated as saer
Other shorthands for Serious Adverse Event Reporting are: SAER
Other shorthands for Serious Adverse Event Reporting are: SAER
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Most popular questions people look for before coming to this page
| Q: A: |
What does saer stand for? saer stands for "Serious Adverse Event Reporting". |
| Q: A: |
How to abbreviate "Serious Adverse Event Reporting"? "Serious Adverse Event Reporting" can be abbreviated as saer. |
| Q: A: |
What is the meaning of saer abbreviation? The meaning of saer abbreviation is "Serious Adverse Event Reporting". |
| Q: A: |
What is saer abbreviation? One of the definitions of saer is "Serious Adverse Event Reporting". |
| Q: A: |
What does saer mean? saer as abbreviation means "Serious Adverse Event Reporting". |
| Q: A: |
What is shorthand of Serious Adverse Event Reporting? The most common shorthand of "Serious Adverse Event Reporting" is saer. |
Abbreviations or Slang with similar meaning
- VAERS - Vaccine Adverse Event Reporting System
- AER - Adverse Event Reporting
- CAERS - CFSAN (Center for Food Safety and Applied Nutrition) Adverse Event Reporting System
- SADE - Serious Adverse Device Effect
- SAE - Serious Adverse Event
- SABRE - Serious Adverse Blood Reactions and Events
- AERC - Adverse Event Reporting Consultants
- CAER - Computerized Adverse Event Reporting
- SAEC - Serious Adverse Event Consortium
- SAER - Serious Adverse Event Reports
- SUAE - Serious Unexpected Adverse Event
- NSAE - non-serious adverse event
- aero - Adverse Event Reporting Ontology
- AERS - Adverse Event Reporting System (Food & Drug Administration)
- SAE(s) - serious adverse event(s)
- AdEERS - Adverse Event Expedited Reporting System
- CAERS - CFSAN Adverse Event Reporting System
- CAERST (CFSAN) - CFSAN Adverse Event Reporting System Team
- FAERS - FDA Adverse Event Reporting System
- MEDWATCH - FDA Safety Information and Adverse Event Reporting Program