Request for Pathology Department Collaboration in a Research Study

Request for Pathology Department Collaboration in a Research Study

<p> Request for Pathology Department Collaboration in a Research Study</p><p>Investigator:</p><p>Department: </p><p>Title of Project: </p><p>Contact Person & Phone Number: </p><p>Duration of project: </p><p>For Investigator </p><p>This study requires the following support (check all that apply) ___ Chemistry specimen (plasma/urine/serum) ___ Blood sample, additional draw ___ Yes ___No ___ Microbiology ___ Histology support - paraffin embedded tissue tissue type: ______Histology support - fresh/fresh-frozen tissue tissue type: ______Pathology review of slides Special sample handling specific for protocol: ___ Yes ___ No Are there any grant, contract, etc. funds available to defray expenses of additional services? ___ Yes ___ No Will investigator be able to coordinate acquisition of specimens (e.g. blood, serum etc) ___ Yes ___ No Describe briefly specimens/services required:</p><p>Frequency of requested services: </p><p>SIGNATURE of Investigator agreeing to participate:______Date: ______</p><p>For Pathology </p><p>Will extra staffing be required? ___ Yes ___ No</p><p>Will services significantly impact upon regular services? ___ Yes ___ No</p><p>Will special procedures be required for sample acquisition? ___ Yes ___ No</p><p>If yes, specify: ______</p><p>Should all pathologists be notified of departmental decision to participate? ___ Yes ___ No </p><p>Pathologist agreeing to participate: (insert name)______has read the IRB proposal and </p><p> agrees to participate. SIGNATURE: ______Date: ______</p><p>Research Director Amila Orucevic, MD, PhD has read the IRB proposal and agrees that histology/pathology</p><p> participation for this study is feasible SIGNATURE: ______Date: ______</p><p>LabCorp designee: (insert name) ______has read the IRB proposal and agrees that</p><p>LabCorp participation is feasible SIGNATURE: ______Date: ______</p><p>Version: 10/23/2014 Note: Final decision to participate is contingent upon investigator securing IRB approval.</p>

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