Tuesday-June-25-2019

<<Back to presentations 

 

Presentations from Tuesday, June 25, 2019

Joint Sessions

8:15PM – 9:00AM – “The Poison Squad: One Chemist’s Single-Minded Crusade for Food Safety at the Turn of the Twentieth Century”

  • Deborah Blum, Director, Knight Science Journalism Program at MIT and Publisher, Undark Magazine

9:00AM – 10:00AM – Using Cannabis from a Medical Perspective

  • Jonathan Gusdorff, DO, DABR, Neuroradiologist and Retail Medical Enterprise Consultant, President, Dr. Jonathan Gusdorff, LLC

Food Sessions

10:30PM – 11:00AM – U.S. Food and Drug Administration Update on Food Policy & Response

  • Frank Yiannas, Deputy Commissioner for Food Policy and Response, U.S. Food and Drug Administration

11:00AM – 11:30AM – Improving the Control of LM in Retail through Surveillance and Partnerships

  • Carl-Martin Ruiz, Deputy Assistant Administrator, Office of Investigation, Enforcement and Audit, Food Safety and Inspection Service, U.S. Department of Agriculture

11:30AM – 12:00PM – Hurricanes from an Industry Perspective

  • Tracy Johnstone, McDonald’s Restaurant Owner Operator
  • Michael Roberson, Director, Corporate Quality Assurance, Publix Super Markets, Inc.

1:30PM – 2:30PM – Regulatory and Industry Partnerships

  • Courtney Bidney, Director, Global Scientific and Regulatory Affairs, General Mills
  • Jessica Badour, Recall Outreach Specialist, Georgia Department of Agriculture
  • Patrick Kennelly, Program Director, Manufactured Food Regulatory Program Alliance, Association of Food and Drug Officials

2:30PM – 3:00PM – FDA’s Strategy for the Safety of Imported Food

  • Donald A. Prater, DVM, Associate Commissioner for Food and Veterinary Medicine, Office of Food and Veterinary Medicine, U.S. Food and Drug Administration

3:30PM – 4:30PM – Reducing Food Waste: Industry and Regulatory Perspectives on Food Recovery Systems

4:30PM – 5:30PM – Advocating for Food Safety with Policy Makers

Drug & Device Sessions

10:30AM – 11:15AM – CDRH’s New Direction in ProductClearance and Compliance: Four New Initiatives that will Affect Industry

  • Adam Saltman, M.D., Ph.D. Medical Officer, Office of Compliance, Center for Devices and Radiological Health, U.S. Food & Drug Administration

11:15AM – 12:00PM – Using Real World Evidence to Speed Medical Device Innovation: An FDA Perspective

  • Douglas Dumont, Office of Surveillance and Biometrics, Center for Devices and Radiological Health, U.S. Food and Drug Administration
  • Adam Saltman, M.D., Ph.D. Medical Officer, Office of Compliance, Center for Devices and Radiological Health, U.S. Food & Drug Administration

12:00PM – 1:30PM – DDC Working Lunch Presentation – Handling FDA Inspections: What to Do When

  • Nancy Singer, President, Compliance-Alliance, LLC
  • Julie Larsen, Principal, Director of Inspection Readiness BioTeknica
  • Courtland Imel, CEO, Ceutical Labs
  • Anne Johnson, District Director, Philadelphia District Office, Program Division Director, Bioresearch Monitoring Division, Office of Bioresearch
  • Monitoring Operations, U.S. Food and Drug Administration
  • Adam Saltman, M.D., Ph.D. Medical Officer, Office of Compliance, Center for Devices and Radiological Health, U.S. Food & Drug Administration
  • Ballard Graham, Retired, U.S. Food & Drug Administration

1:30PM – 2:10PM – What You Need to Know About Promoting Quality with a Proactive CAPA System

  • Lynne Melendez, Director CAPA Management, Janssen

2:10PM – 3:00PM – Getting Ready to Implement the New EU Device Regulation

  • Paul Brooks, Executive Director, Regulatory Affairs Professional Society

3:30PM – 4:10PM – CDC Update Fungal Meningitis Outbreak: a CDC perspective/Burkholderia Cepacia Multi-State Outbreaks Related to Drugs, Devices and Cosmetics Used in Healthcare Settings

4:10PM – 4:50PM – Working Together: Learn How You Can Participate in FDA/Industry Training Partnerships

  • Captain Jane Kreis, Training Officer, Pharmaceuticals, U.S. Food and Drug Administration

4:50PM – 5:30PM – Compliance Panel – Get Your Questions Answered

  • Alonza Cruse, Director of the Office of Pharmaceutical Quality Operations, U.S. Food & Drug Administration
  • Adam Saltman, M.D., Ph.D. Medical Officer, Office of Compliance, Center for Devices and Radiological Health, U.S. Food & Drug Administration
  • Anne Johnson, District Director, Philadelphia District Office, Program Division Director, Bioresearch Monitoring Division, Office of Bioresearch Monitoring Operations, U.S. Food and Drug Administration
  • Captain Jane Kreis, Training Officer, Pharmaceuticals, U.S. Food and Drug Administration

Retail Sessions

1:30PM – 3:00PM – 2019 Risk Factor Study Learning Lab: Connect the Dots and Using Collaboration to Reduce Risk Factors

  • Chris Smith, Director, Retail Food Protection Branch III, U.S. Food and Drug Administration
  • Andre Pierce, Director, Division of Environmental Health & Safety, Wake County Government, North Carolina
  • Jason Reagan, Program Manager, Gwinnett, Newton & Rockdale Counties, Georgia
  • Mark Speltz, Bureau Chief, Food and Consumer Safety Bureau, Iowa Department of Inspections and Appeals

3:30PM – 4:15PM – Food Safety Management Systems

  • Robert Garfield, Chief Food Safety Assessment Officer & SVP, Safe Quality Food Institute
  • LeAnn Chuboff, Vice President Technical Affairs, Safe Quality Food Institute

4:15PM – 5:30PM – When Food Science Meets Behavioral Science: Changing Behavior for Good

  • Jennifer J. Tabanico, President, Action Research
search previous next tag category expand menu location phone mail time cart zoom edit close