Back to Results
First PageMeta Content
Medicine / Institutional review board / Clinical trial / Investigational New Drug / Office for Human Research Protections / Human subject research / Public Responsibility in Medicine and Research / Clinical research coordinator / Cooperative Human Tissue Network / Clinical research / Research / Science


NOTE: THIS GUIDANCE REPLACES OHRP’S JULY 11, 2002 GUIDANCE ENTITLED “GUIDANCE ON WRITTEN IRB PROCEDURES
Add to Reading List

Document Date: 2014-09-05 00:37:00


Open Document

File Size: 150,71 KB

Share Result on Facebook

Company

IRB Review / /

Country

United States / /

/

IndustryTerm

risk protocols / written protocol / /

Organization

Institutional Review Board / Office for Human Research Protections / U.S. Food and Drug Administration / Human Research Protections Department of Health and Human Services Guidance / Department of Health and Human Services / /

/

Position

investigator / official / Governor / Agency head / chairperson / independent observer / /

Technology

high-risk protocols / research protocol / HHS-approved protocol / written protocol / /

URL

http /

SocialTag