We’re not surprised if you’ve asked yourself this question before. Unfortunately, the answer is yes. However, we try to make our forms as simple as possible. This is why we redesigned the Formaldehyde Questionnaire based on feedback received from in-person interactions, through email, or the EHSO customer satisfaction survey. This article explains the EHSO Formaldehyde Questionnaire and monitoring program. You are […]
-
Recent Articles for Emory’s Research Administrator
- Message from VPRA, Dr. Robert Nobles (March 2024)
- RGC Policies Summary
- Biological Safety Protocol Electronic Submission
- Sponsored Research: The Importance of Obtaining Approvals Before Starting Work
- RCRA Minimizing Administrative Burden While Maintaining Compliance
- OTT Plans to Introduce New and Improved Process for Outgoing Low-Risk DUAs
- Occupational Health Services (OHS)
- Research Compliance News and Updates (January 2024)
- HHS Office of Research Integrity (ORI) Notice of Proposed Rule Making (NPRM)
- NIH Workplace Conduct Requirements
New from NIH
- Exploring the Difference Between Exempt Human Subjects Research and Expedited IRB Review April 25, 2024We’ve heard that there is some confusion about exempt human subjects research and expedited IRB review. Expedited review is not the same as exempt research. Here are a few points to provide clarity.NIH Staff
- Exploring the Difference Between Exempt Human Subjects Research and Expedited IRB Review April 25, 2024
News from the Office of Technology Transfer
Emails from EHSO