Medical Research

UH/NJMS Clinical Research Study Initiation Form

Office of Clinical Research Administration (OCRA).Study Feasibility Form.In order to initiate a clinical research study at UH/NJMS, submission of this form to the OCRA, , as part of the study initiation package for compliance in billing of clinical services for research studies

Standard Operating Procedures s13

Standard Operating Procedures s13

GENERAL INFORMATION.CRS personnel do not support submission into CRPC and have been instructed to refer submission requests to Julie Haney at ext 3340 or pager 541-6900 pin 4268.i2 Links are only accessible to RPCI appointed faculty and staff with intranet access granted

Clinical Research Ethics Consultation Request

Clinical Research Regulatory and/or Ethics.Consultation Request Form.To request a clinical research regulatory and/or ethics consultation, please complete the information below and email the completed form to

TIP Sheet INVESTIGATIONAL DEVICE EXEMPTION APPLICATION (IDE)

TIP Sheet INVESTIGATIONAL DEVICE EXEMPTION APPLICATION (IDE)

Subject: Clinical Trials Registration New Federal Requirements - Important Message from Gordon R

Subject: Clinical Trials Registration New Federal Requirements - Important Message from Gordon R. Bernard, Assistant Vice Chancellor for Research.Dear Fellow Investigators.This e-mail is to inform you of the newly enacted law promulgated by Congress regarding

Niehs Irb Standard Format for Protocols

Protocol Standard Format Page 5.INSTITUTIONAL REVIEW BOARD.TALLAHASSEE MEMORIAL HEALTHCARE.STANDARD FORMAT FOR PROTOCOLS.for submission with Initial Review Application.In order to avoid the submission of incomplete protocols which may lead to delay in

IRB Review Checklist

IRB Review Checklist.Attached are checklists to assist IRB members in their review of.2. Consent forms.4. Consent forms for research involving genetic testing additional requirements.5. HIPAA authorization.6. Waiver of consent and/or authorization.8. Obtaining Consent and Capacity Assessments

University of Pittsburgh Guideline: Study Documentation for FDA Regulated Research

University of Pittsburgh Guideline: Study Documentation for FDA Regulated Research.Data integrity is vital in the conduct of clinical research because data is necessary for the evaluation, reconstruction, and validation of clinical findings, observations

New Irb Research Application Submission Form

New Irb Research Application Submission Form

NEW IRB RESEARCH APPLICATION SUBMISSION FORM.APPLICATION CHECKLIST FOR A NEW HUMAN SUBJECTS RESEARCH PROJECT.ALL NEW APPLICATIONS MUST INCLUDE A COPY OF EACH OF THE FOLLOWING.New IRB Research Application Submission Form including Abstract (Study Rationale) and Synopsis.Consent Form if required

Harnessing Inclusive Urban Knowledge for the Implementation of the New Urban Agenda s1

Research outputs.Listing of Research outputs.Harnessing inclusive urban knowledge for the implementation of the New Urban Agenda.Robin, E., Steenmans, K. A. & Acuto, M. 2019 In : Journal of Urban Research & Practice.Research output: Contribution to journal Article

Insert Dod Seal Here

Department of the Navy Human Research Protection Program.Institutions Engaged in Research with Human Subjects.with an Internal IRB.Directions for Renewing an Assurance for a Command with an IRB

Genome-Wide Association Study of Copy Number Variations (Cnvs) with Opioid Dependence

Genome-wide Association Study of Copy Number Variations (CNVs) With Opioid Dependence.Running Title: First CNV Study of Drug Dependence.Dawei Li1,2,3,4*, Hongyu Zhao5,6, Henry R. Kranzler7, Ming D. Li8, Kevin P. Jensen1, Tetyana Zayats1, Lindsay A. Farrer9, and Joel Gelernter1,6,10

Investigator Handbook

INVESTIGATOR HANDBOOK.FIRST TIME SUBMISSION 5.EDUCATIONAL REQUIREMENTS 5.NEW SUBMISSIONS 5.FOR SINGLE SUBMISSIONS 5.FOR MULTICENTER SUBMISSIONS Submitted by Sponsor/CRO: 6.MULTICENTER SUBMISSION Packet for Principal Investigator: 6.VULNERABLE POPULATIONS 7.STATE REQUIREMENTS FOR RESEARCH 7

Guidelines for Case Reports

Institutional Review Board (IRB).GUIDELINES FOR CASE REPORTS.Federal regulations (45 CFR 46.102) define research as a systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable

Institute of Translational Health Sciences (Iths)

INSTITUTE OF TRANSLATIONAL HEALTH SCIENCES (ITHS).UW CLINICAL RESEARCH CENTER (CRC) REQUEST FOR SERVICES.Complete this registration if you wish to use the ITHS UW CRC and/or any affiliated cores or resources.If you have questions please email or contact the CRC Program Manager at (206) 598-4730

Boston University Medical Center s1

Clinical and Translational Science Institute.General Clinical Research Unit.APPLICATION FOR USE.Certification of Acceptance.I hereby certify that the statements, herein, are true and complete to the best of my knowledge and accept the obligation to comply

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