Industry News & Updates

21 CFR 50.20 & Non-English Speaking Subjects
Thursday, Jun 7, 2012
Altering Medical Device Recalls
Wednesday, Jun 6, 2012
Will Voluntary Audits Help the FDA?
Tuesday, Jun 5, 2012

Is Your Trial Complex?

New!

Recognize five key areas that can complicate medical device trials.

Download Now

Significant Risk / Non-
Significant Risk Determination

Determine the risk and
exemptions of
device studies.
Download Now

510(k) Clinical
Data Requirements

Status & Considerations
for Clinical Studies

Download Now