Application of ADME/PK Studies to Improve Safety Assessments for Foods and Cosmetics
Register now to participate in “Application of ADME/PK Studies to Improve Safety Assessments for Foods and Cosmetics” on February 23. Registration closes February 18 for those attending on-site at the Wiley Auditorium, US Food and Drug Administration (US FDA), College Park, Maryland. Registration for the webcast will continue until the event.
Presentations
Overview: Value of ADME/PK Studies in Safety Assessment
Harvey Clewell, The Hamner Institutes for Health Sciences, Research Triangle Park, North Carolina
The Importance of ADME/PK to Inform Human Safety Assessments Based on Animal Studies: Example with Furan
Greg Kedderis, Independent Consultant, Research Triangle Park, North Carolina
The Role of ADME/PK in the Extrapolation of In Vitro Toxicity Results to Equivalent In Vivo Exposures: Where it Started with the Acrylamide Example and Where We are Now
Bas Blaauboer, Institute for Risk Assessment Sciences, Utrecht University, Utrecht, The Netherlands
Consideration of ADME/PK in Safety Assessments for Engineered Nanomaterials: Example with Silver Nanoparticles
William Boyes, USEPA/NHEERL, Research Triangle Park, North Carolina
Roundtable Discussion: Issues for Use of ADME/PK in Safety Assessments for Foods and Cosmetics
Harvey Clewell, moderator; all speakers participate
This series provides scientific training that is high-quality, cutting-edge, future-oriented toxicological science to provide a well-grounded, foundation to inform the work of US FDA employees and others. This event is not a public forum for discussion of toxicology regulatory issues. Scheduled from 8:15 am–12:30 pm, registrants can participate onsite at the FDA Wiley Auditorium, College Park, Maryland, or by viewing the webcast.