Join us for an interactive introduction to best practices in preparing for and participating in clinical trial monitoring visits.
Keyword: Clinical Trial
Independent monitoring for IND/IDE investigator-initiated clinical trials
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
Engage with data analysis experts to ensure rigor in your clinical and translational research