Word |
PDF |
Revised/Effective
Date |
|
 |
Adverse Event
Reporting Form |
05/22/2006 |
|
| Adverse
Event Summary and Baseline Demographics and Relevant Clinical
Characteritics, by case (Microsoft Excel) |
02/15/2006 |
||
|
Patient
Enrollment Summary for Device Studies |
02/15/2006 |
|
|
Patient
Enrollment Summary for Drug Studies |
02/15/2006 |
|
 |
Reviewer's Worksheet | 03/23/2007
|
|
|
Investigator's Interim Data and Safety Monitoring Report |
03/23/2007 |
|
 |
Monitoring Review Process Flow Chart | 02/23/2007 |
KUMC Wichita | Research Institute | Research Advisory Council
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The University of Kansas Medical Center