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This is an archive of the Task Force on Adverse Health Events website, which was last updated in December 2008, and will not be updated further. If you have difficulty accessing any material, please contact Executive Council.

Frequently Asked Questions (FAQ)

  1. How does the Office of the Task Force on Adverse Health Events differ from the Commission of Inquiry on Hormone Receptor Testing?
  2. What is the relationship of the Task Force on Adverse Health Events with the Department of Health and Community Services?
  3. What is the relationship of The Task Force on Adverse Health Events with Regional Health Authorities (RHAs)?
  4. How can interested individuals provide input/participate?
  5. Will The Task Force release a final report? Will it become public?

 

1. How does the Office of the Task Force on Adverse Health Events differ from the Commission of Inquiry on Hormone Receptor Testing?

The Task Force on Adverse Health Events is a separate process from the Commission of Inquiry on Hormone Receptor Testing. The Task Force will not consider matters related to hormone receptor testing or any other complaints or problems with specific adverse events. Rather it will look at how to improve policies and procedures for managing adverse events after they occur.

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2. What is the relationship of the Task Force on Adverse Health Events with the Department of Health and Community Services?

The Task Force on Adverse Health Events is chaired by the Secretary to Cabinet (Health Issues) who is employed with the Executive Council Office of the provincial government. While the Task Force is not part of the Department of Health and Community Services, the report of the Task Force will focus exclusively on matters within the health and community services system.

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3. What is the relationship of The Task Force on Adverse Health Events with Regional Health Authorities (RHAs)?

The Task Force is consulting closely with RHAs to gather information and receive input. The recommendations of the Task Force will be directly relevant to RHAs, so it is important to have regular interaction with their representatives. A Health System Liaison Committee has been established to facilitate consultation.

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4. How can interested individuals provide input/participate?

Interested individuals/groups can participate in a call for submissions. In addition, health system stakeholders, including patient advocacy groups, health professional associations, unions, researchers and teaching/learning organizations have been invited to participate in the Provincial Forum on Adverse Health Events in St. John’s on May 26, 2008.

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5. Will The Task Force release a final report? Will it become public?

The Task Force on Adverse Health Events will submit a final report to government during the summer of 2008. As per government policy, all reports will become public within 30 days of receipt.

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