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Working Towards Harmonization in Medical Device Regulation |
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| GHTF > Meetings and Training > Conferences >8th GHTF Conference - Ottawa, Canada 18-22 September 2000 > PVC: Expert Review and Considerations for the Future Panel Session Brief |
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Title of Panel Session:
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PVC: Expert Review and Considerations for the Future |
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Time:
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Wednesday, 20 September 2000 9:00 am - 11:30 am |
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Chair:
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John S. Parks VP, Regulatory and Quality Baxter Corporation |
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Panel Participants:
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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) |
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| Speaker, TBA United States Food and Drug Administration |
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| Speaker, TBA National Toxicology Program |
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| Speaker, TBA EUCOMED |
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Topic:
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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
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