• UC Home
  •  |
  • Visit UC
  •  |
  • Support UC
  •  |
  • Directories
  •  |
  • UC Search
  •  |
  • UC Tools
    • Blackboard
    • OneStop
    • Libraries
    • Student Email
    • UCMail
    • UCFileSpace
    • E-Professional
    • UC Flex/ESS
  • Research Compliance
  • Biosafety
 
  • Research Integrity Home
  • Human Subjects Research
    • Overview
    • IRB
      • Overview
      • ePAS Overview
      • Board Consolidation
      • FDA Training Information
      • Scientific Review
      • External Submissions
      • Fee for Industry Sponsored IRB Review
      • Indemnification Policy
      • News and Announcements
      • CITI Requirements
      • Forms for Modification
      • Miscellaneous Reporting/Information
      • About UC's IRB
      • Especially For
      • Policies and Procedures
      • Reporting Concerns
    • HRP
      • Overview
      • Information for Research Participants
      • Definition of Key Personnel
      • SOP Templates
      • Required Training
      • Research Policies
      • Regulatory Links
      • Roles and Responsibilities
    • HIPAA
      • Overview
      • Frequently Asked Questions
      • Authorization Forms
      • Data Use
      • HIPAA Privacy Glossary of Terms
      • Training
      • Reporting Concerns
      • Useful Links
    • PAM Program
      • Overview
      • Frequently Asked Questions
      • Regulatory Mandates
      • Policies
      • Links
    • IND/IDE Assistance
      • Overview
      • Definitions
      • Policies
      • Monitoring
      • Investigational New Drug (IND)
      • Investigational Device Exemption (IDE)
      • FAQs
    • ClinicalTrials.gov
    • External Submissions
      • Overview
      • WIRB
        • Overview
        • UC and Western IRB (WIRB)
        • How to Submit to WIRB
        • Consent Form
        • FAQs
      • SAIRB
        • Overview
        • Schulman Background
        • How to Submit to SAIRB
        • Consent Form
        • FAQs
    • Reporting Concerns
  • Institutional Review Board
  • IACUC
    • Overview
      • LAMS
    • FAQs
    • Regulatory Mandates
    • Protocol Submissions
    • Quick Forms
    • IACUC Policies
    • Training & Personnel
    • Occupational Health & Safety
    • Reporting Concerns
    • Grant Submissions
    • Links
  • Biosafety
    • Overview
    • IBC FAQs
    • Human Gene Transfer
    • Submit IBC Protocol for rDNA and Biohazardous Materials
    • IBC Meetings
    • Regulatory Mandates
    • Core Facilities
    • Safety Fact Sheets
    • Biosafety Manual
    • Biosafety and Biosecurity
    • Genetically Modified Animals Registry
    • Training
    • Select Agents and Toxins
    • Reporting Concerns
    • Grant Submissions
    • Staff
    • Links
  • Radiation Safety
    • Our Mission
    • FAQs
      • Administrative
      • Dosimeter/Monitoring
      • General
      • RAM Waste
      • Surveys
      • Training
    • Manuals, QMP & Policies
    • Staff Listing
    • Forms
    • News & Events
    • Training
      • Videos
      • Schedules
        • RAM Radiation Worker
        • Health Care Worker
    • Request a Special Survey
    • Isotope Fact Sheets
    • Request a Waste Pick up
    • Links
  • Contact Us
  • Research Home

Biosafety

  • Biosafety
    • Overview
    • IBC FAQs
    • Human Gene Transfer
    • Submit IBC Protocol for rDNA and Biohazardous Materials
    • IBC Meetings
    • Regulatory Mandates
    • Core Facilities
    • Safety Fact Sheets
    • Biosafety Manual
    • Biosafety and Biosecurity
    • Genetically Modified Animals Registry
    • Training
    • Select Agents and Toxins
    • Reporting Concerns
    • Grant Submissions
    • Staff
    • Links

Safety Fact Sheets

  • Q-Fever (PDF)
  • Respiratory Protection (PDF)
  • Biosafety Cabinets and Bunsen Burner (PDF)

Copyright Information © 2013 University of Cincinnati
51 Goodman Drive, University Hall Suite 540, ML0567, Cincinnati, OH 45221-0567
Phone (513) 558-5034   |   research.compliance@uc.edu   |   Contact Us