Following on from the second webinar in this 4-part series, "Quality In, Quality Out: Regulatory Drivers of Supplier Quality Management in the Medical Device Industry," this third presentation will take a specific and deeper dive into the regulatory requirements for supplier management for the pharmaceutical and biopharma industries.

Leverage New Tools for Device CAPA Compliance
**FDAnews Virtual Conference**
Dec. 19, 2013 — 10:00 a.m. - 4:00 p.m. EST
www.fdanews.com/DeviceCAPAVCPR3