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Child Death Review Case Reporting System Data Use Agreement
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2016-04-05 10:00 AM - Commissioners' Agenda
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Child Death Review Case Reporting System Data Use Agreement
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Last modified
4/7/2018 10:41:46 AM
Creation date
4/7/2018 10:39:05 AM
Metadata
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Template:
Meeting
Date
4/5/2016
Meeting title
Commissioners' Agenda
Location
Commissioners' Auditorium
Address
205 West 5th Room 109 - Ellensburg
Meeting type
Regular
Meeting document type
Supporting documentation
Supplemental fields
Alpha Order
p
Item
Request to Approve a Child Death Review Case Reporting System Data Use Agreement between the Michigan Public Health Institute and the Kittitas County Public Health Department
Order
16
Placement
Consent Agenda
Row ID
28675
Type
Agreement
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C. Physical security: In addition to electronic security, the devices on which the dataset have <br />been copied must be physically secured to prevent theft of the device. Describe below the <br />physical security measure in place for each device. <br />If co -investigators at different institutions from the PI will also have physical control of <br />the data, complete the table for each such co -investigator's institution and describe how <br />data will be securely transferred between institutions. <br />Y. Receiving Institution <br />A. Identify the Receiving Institution, as that term is described in the Guidelines. <br />B. Provide the IRB assurance number. <br />C. Describe your Institution in detail. What kind of work does it do? Include the type of <br />organization, its profit/non-profit status, and primary sources of revenue. <br />D. Provide evidence in an attachment that your institution is registered with the U.S. <br />Office for Human Research Protections. <br />E. Describe your plans to obtain IRB approval for this study using the NCRPCD data. <br />F. Describe your Institution's experience in overseeing the use of sensitive research data <br />by its staff. Please give specific examples. <br />G. Describe any known breaches of sensitive research data by your organization and the <br />steps taken to remedy the breach. <br />23 <br />Location of Device <br />Description of physical security <br />ID <br />Indicate building <br />name and office <br />Examples are offices are locked when unoccupied; storage in secure <br />number <br />cabinets when the device is not in use; and monitored access to the <br />building where the data are stored. <br />1 <br />2 <br />3 <br />4 <br />Y. Receiving Institution <br />A. Identify the Receiving Institution, as that term is described in the Guidelines. <br />B. Provide the IRB assurance number. <br />C. Describe your Institution in detail. What kind of work does it do? Include the type of <br />organization, its profit/non-profit status, and primary sources of revenue. <br />D. Provide evidence in an attachment that your institution is registered with the U.S. <br />Office for Human Research Protections. <br />E. Describe your plans to obtain IRB approval for this study using the NCRPCD data. <br />F. Describe your Institution's experience in overseeing the use of sensitive research data <br />by its staff. Please give specific examples. <br />G. Describe any known breaches of sensitive research data by your organization and the <br />steps taken to remedy the breach. <br />23 <br />
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