Plan on joining us at the Indiana Medical Device Manufacturers Council (IMDMC) event entitled “Regulatory 101” on May 15, 2014. Gretchen Bowker, COO of Pearl Pathways will be speaking at the event at the Montage Banquet Hall in Indianapolis, Indiana. This is a full day event and is appropriate for staff who are relatively new to the FDA regulatory world or those who need a FDA refresher. Gretchen will be presenting at 1:30 on Clinical Trials and IDE’s. To register for the event click here and to visit the IMDMC website, see this link.
Navigating Institutional Review Board (IRB) Oversight
Read the latest publication from our IRB co-chair.
Clinical Research Accelerated
You need high quality, timely board reviews so that you can get your study in the clinic.