A guide for diligent management of IRB applications and reporting obligations through meticulous documentation and tracking of responsibilities
Keyword: IRB
Expert management consultation services that deliver customized solutions for planning, initiating, and overseeing your projects
Guidance in assessing if you need an investigational new drug (IND) or investigational device exemption (IDE) for your study
Support and expertise to prepare and submit investigational new drug (IND) and investigational device exemption (IDE) pre-submission meeting requests to the FDA
Support and expertise to prepare and submit investigational new drug (IND) and investigational device exemption (IDE) applications to the FDA