Webinar Archive

To purchase a webinar archive please click onthe title(s) you are interested in below.

Wednesday, September 14, 2016 - 11:00am to 1:00pm

Every regulatory professional should know the standards, groundwork, expertise and technology required to submit compliant eCTD submissions to FDA.

Wednesday, January 18, 2017 - 11:00am

Gain the knowledge and skills to develop, compile, and communicate validation documentation that meets the needs of the customer and the requirements of the standard.

Friday, March 3, 2017 - 11:00am to 11:30am

(FREE) The how and why of excipient education from the ELL, and answer any questions you may have.