Washington, DC
January 30, 2012 -February 2, 2012
Keynote Address
Janet Woodcock, FDA, MD
Keynote Address
Peter Kim, Merck Research Laboratories, PA
SESSIONS:
- Advancing Risk Assessment Approaches in the 21st Century
- Recent Successes and Future Challenges in Accelerating Implementation of the NRC Tox 21 Report
- Patient Risk Assessment Based on Carcinogenicity Evaluation of Pharmaceuticals
- Irradiation in the Production, Processing and Handling of Food: The U.S. Framework
- Threshold of Toxicological Concern: Designs, Domains, and Databases
- Improving our Understanding of the Cancer Risk Posed by Hexavalent Chromium in Drinking Water
- When Epidemiology and Toxicology Collide: Navigating the Path Forward for Formaldehyde
- Use of New Data on the Former Fuel Additive, MTBE, in Hazard Identification and Risk Assessment
UPDATES:
- NTP Workshop: Role of Environmental Chemicals in the Development of Diabetes and Obesity
- FDA’s Guidance for Industry on Reproductive and Developmental Toxicities
- The ELSIE Database: Extractable, Leachable and Knowledge Sharing Amongst Pharmaceutical Companies and Regulators
- FDA’s Dietary Supplements Office: New Director/New Directions
- FDA’s Medical Countermeasures (MCM) Initiative: Responding Faster and More Effectively toBioterrorism and Infectious Diseases
- A Therapeutic Intervention that Mitigates Intestinal Acute Radiation Poisoning
- Protecting the U.S. Food Supply from Foods Contaminated with Radionuclides From a Nuclear Reactor Accident?