IRB Submissions

Clinilabs’ regulatory staff are experts at preparing and submitting IRB applications.  We have worked with a variety of IRB’s and ethics committees worldwide in order to complete applications for single and multi center studies.  In North America, Clinilabs utilizes New England IRB, which completed a routine audit of our organization in 2011, with no observations.

 

Click HERE to download our Multicenter, Full Service CRO Case Study.