Welcome to Registration
The Center for Biofilm Engineering is pleased to bring our annual regulatory meeting Biofilm Technologies: Pathways to Product Development to you in a virtual format.
As is the case when we are able to meet in person, the goal of this meeting is to engage industry, academia, and federal agencies on the impact of biofilm in our daily lives. Over the past decade, academic research advances and private company R&D efforts have led to the development of innovative anti-biofilm technologies with transformative potential in the consumer products and healthcare arenas. Likewise, advances in methods for studying and assessing biofilms have provided new insights into important biofilm characteristics such as why biofilms are difficult to kill and remove from surfaces. The CBE is sponsoring this meeting for the eighth consecutive year in an effort to bring together industry, regulatory agencies, and academia to discuss biofilm-related technologies, research, and regulatory pathways. There will be two sessions—Medical Technologies and Surface Technologies—with presentations relating to products regulated by both EPA and FDA.
Sessions will convene from 9:15 a.m.–2:00 p.m. MST each day, with ~30-minute presentations to be delivered via WebEx Events. Each presentation will feature live Q/A time and we will have a discussion panel at the end of each day.
|Non-Member 3 Day Pass||
|Non-Member 1 Day Pass||