Informed Consent for Laboratory Testing

Guidelines for Clinicians: The Consent Process for SARS-CoV RT-PCR and EIA Testing at CDC and Public Health Laboratories (Jan 8, 2004) Read This First
Appendix F3, Supplement F of Public Health Guidance for Community-Level Preparedness and Response to SARS
Fact Sheet for Clinicians: Interpreting SARS-CoV Test Results from CDC and Other Public Health Laboratories (Jan 8, 2004)
Appendix F7, Supplement F of Public Health Guidance for Community-Level Preparedness and Response to SARS
Consent Forms (before testing)
- EIA (antibody) Testing
- RT-PCR Testing
Patient Information (after testing)
- EIA (antibody) Testing
- RT-PCR Testing
CDC letter regarding local IRB issues (Jan 8, 2004)

Page last reviewed: May 3, 2005
Page last updated: May 3, 2005
Content source:
- National Center for Immunization and Respiratory Diseases , Division of Viral Diseases

Top