Reed Smith is pleased to announce a fall "back to school" webinar series on a variety of topics of interest to our FDA-regulated clients. CLE credit is available in certain jurisdictions.
Reed Smith announces fall FDA webinar series image

On Thursday, October 10, partner Rachael Pontikes and senior associate Emily Hussey will present a webinar on “FDA inspections of health care facilities: How to keep calm and carry on when the FDA walks through your door.” The webinar will discuss the ins and outs of FDA inspections of health care facilities, including pharmacies, distributors and similarly FDA-regulated health care facilities.

On Wednesday, October 30, partner Cori Annapolen Goldberg, counsel Marc Hauser, and associate Adam Brownrout will present “CBD: What now?” This webinar will present an overview of current federal (FDA, USDA) and state regulations for CBD and CBD products.

On Wednesday, November 13, partner Celeste Letourneau and associate Rebecca Dittrich will present a webinar on “Clinical trials and contracts: Rationale and regulations explained.” A clinical trial contract establishes the responsibilities and rights between the parties for the conduct of a clinical trial. This webinar will address the regulations and rationales underpinning the terms commonly included in a clinical trial agreement to inform negotiation and execution of the agreement.

To learn more or to register for any webinar in this series, please contact Webinar Requests.

For more information on the webinar series, or to suggest a topic for a future FDA webinar, please contact Elizabeth Starrantino.