Ms. Davenport counsels clients on a wide variety of FDA issues, with a focus on the medical device area. She has advised clients on matters relating to clinical investigations, pre-market submissions, pre-and post-market compliance, product exporting and importing and the Good Manufacturing Practices regulations. Ms. Davenport also advises companies with regard to food and dietary supplement matters.
Ms. Davenport regularly assists with conducting due diligences of medical device and drug companies, and has provided FDA-related litigation support.
Ms. Davenport is a member of the American Bar Association, the Maryland State Bar Association and the District of Columbia Bar.
Prior to joining Goodwin, Ms. Davenport was an associate in the FDA Department at WilmerHale.