Case Study

VERO Biotech Gains FDA Approval for Complex Drug and Device Combination

Anxious to move forward and bring its drug and delivery device to market, VERO Biotech was faced with a daunting 510K filing process with the Food and Drug Administration (FDA). VERO Biotech enlisted the help of Advarra Consulting to provide a comprehensive strategic and tactical project plan.

Download the case study to learn more about how VERO Biotech leveraged Advarra Consulting to successfully navigate the pathway to FDA approval.

Who Should Watch?

CEU Credits

Certificate of Attendance

Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

Download Now