Overview

Do you work on clinical trial issues and would like to know more about the core scientific principles? Need a review on how to interpret clinical trial results? This webinar will discuss fundamentals of clinical trials. Topics include understanding the basics of clinical trial design and interpretation, how to quickly read published clinical trial results, an overview of types of clinical trials, ranging from superiority to non-inferiority designs, and why participant diversity is important. 

Speakers

Margo Heath-Chiozzi, Senior Vice-President, Regulatory Affairs, Celldex Therapeutics, Inc
Lance L. Shea, Partner, BakerHostetler
Robert J. Temple, Deputy Center Director for Clinical Science, CDER
Moderated by Brian J. Malkin, Partner, McDermott Will & Emery

Register

Webinar

$99
  • +$100 for non-members

Webinar & Recording

$149
  • +$100 for non-members
Register Now

Internet Explorer and Microsoft Edge are not supported by the checkout process.

Please use Chrome, Firefox, or Safari.  If you are unable to use these browsers, please contact us at 202-371-1420 or [email protected] and we will assist you.

An access link will be provided to attendees via email upon registration.

If you are registering on behalf of someone else, the link to access the webinar will go to the email address provided at the point of registration.

Those registering on the day of the webinar will receive an access link via email upon successful payment.

We use Zoom to conduct webinars which works on most devices. You may participate in the webinar on a mobile device via the Zoom App or by dialing in. If you require the dial in information, please contact Coleen Carney at [email protected].

Test your device: https://support.zoom.us/hc/en-us/articles/201362193-Joining-a-meeting

Webinar recordings are sent via email as soon as we are able to process and verify the quality of the recording. This usually occurs within 3 business days of a webinar broadcast.

If multiple people at your organization wish to participate from separate devices, each will be required to purchase access.

Summer Learning Series

The Summer Learning Series brings the top thinkers and leaders of our industry to speak on a broad array of topics essential to the food and drug law professional, covering matters that perhaps we all wish we knew a bit more about as we work and converse with clients, colleagues, and the FDA. Join us this June through July and build foundation in the following subjects: