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         1992 - 
Global Harmonization Task Force
(Flags: European Union, United States of America, Canada, Australia, Japan)
Working Towards Harmonization
in Medical Device Regulation

PVC: Expert Review and Considerations for the Future Panel Session Brief

8th GHTF Conference - Ottawa, Canada

18-22 September 2000

PVC: Expert Review and Considerations for the Future
Panel Session Brief

This brief is also available in Word and PDF format.

Title of Panel Session:
PVC: Expert Review and Considerations for the Future
Time:
Wednesday, 20 September 2000
9:00 am - 11:30 am
Chair:
John S. Parks
VP, Regulatory and Quality
Baxter Corporation
Panel Participants:
Irwin Hinberg, PhD
Health Canada
Device Surveillance Division
Medical Devices Bureau
  Jon Cammack, PhD
PVC Taskforce
Research Director, Baxter Healthcare Corporation
AdvaMed (Advanced Medical Technology Association)
  Speaker, TBA
United States Food and Drug Administration
  Speaker, TBA
National Toxicology Program
  Speaker, TBA
EUCOMED
Topic:

Panelists will discuss the following: The National Toxicology Program Research (NTP) and findings regarding the PVC DEHP issue; the Health Canada and US Food and Drug Administration review and findings regarding PVC; European concerns and approaches to dealing with the environmental, health and safety issues and concerns regarding PVC and DEHP; the industry study of the safety of poly vinyl chloride issues in response to issues raised over the years; industry response to health and safety concerns; and the future of PVC and non PVC materials in drug containers and medical devices.

Regulators and manufacturers of medical devices and pharmaceutical packager utilizing poly vinyl chloride will benefit from the panel presentations and open discussion regarding recent assessments of safety of PVC and phthalates.

Updated 22 July 2004