C-TASC is an experienced CRO for the NHLBI in the BABY HUG study.  As such, C-TASC has been responsible for submitting all of the required materials for FDA review of this clinical trial. C-TASC knowledge about the internal review system at the FDA combined with the  recent hire of a regulatory expert in FDA submissions ensures that C-TASC staff will be more than able to prepare all of the required regulatory submissions to the FDA.