Ready Your Laboratory for the FDA’s Stage 1: Corrective Action and Removal Reporting

Part three of a six-part webinar series.

Learn the necessary steps to comply with the FDA requirements for corrective action and removal reporting specific to laboratory developed tests. In order to help laboratories prepare for the FDA final rule, speakers will provide context relevant to laboratories and share practical solutions.

Speakers

• Bobbi S. Pritt, MD, FCAP, chair, Council on Scientific Affairs
• Earle S. Collum, MD, FCAP, chair, Council on Accreditation
• Deeona R. Gaskin, J.D., MPH, partner, Sidley Austin