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Irb Student published presentations and documents on DocSlides.

Good Clinical Practices

Good Clinical Practices

  • pamella-moone
  • 53 Slides

Presented By :. Version: 1.0/2017. 1. Good clinic...

Stony Brook University

Stony Brook University

  • tatyana-admore
  • 12 Slides

The Process for Joining TIES. Project Team:. PI ...

ROAD MAP: Getting a Cancer Study Done at Jefferson

ROAD MAP: Getting a Cancer Study Done at Jefferson

  • ellena-manuel
  • 0 Slides

Sylvia O’Neill, MD. Associate Director of Regul...

UC DIG REF CONFERENCE CALL

UC DIG REF CONFERENCE CALL

  • pamella-moone
  • 0 Slides

AGENDA. Monday March 30, 2015 . 1. .) . Reporting...

Objectives 1. Define and describe each of the Agreement types being discussed today;

Objectives 1. Define and describe each of the Agreement types being discussed today;

  • test
  • 0 Slides

2. Highlight specific questions to ask when dete...

1 Updating the Common Rule Governing Human Subjects Research Protections

1 Updating the Common Rule Governing Human Subjects Research Protections

  • tawny-fly
  • 0 Slides

Jerry Menikoff. 2. 2. Disclaimer. The views expr...

© HRP Consulting Group Investigator Responsibilities in Human Subjects Research

© HRP Consulting Group Investigator Responsibilities in Human Subjects Research

  • liane-varnes
  • 0 Slides

Jeffrey M. Cohen, Ph.D. CIP. Chief Executive Offi...

cHildren’s Findings An IRB

cHildren’s Findings An IRB

  • cheryl-pisano
  • 0 Slides

Infoshort. November . 2012.

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•••••••••••••••••••••••••••••••••

  • danika-pritchard
  • 0 Slides

University of Kentucky E-IRB. Application Feature...

How to submit an amendment to a project that has already received IRB approval

How to submit an amendment to a project that has already received IRB approval

  • pasty-toler
  • 0 Slides

Submitting an Amendment. Step 1: Log into IRBMana...

Preparing for your Research

Preparing for your Research

  • jane-oiler
  • 0 Slides

Project. Christopher Kabir, MS. PCOR Coordinator....

Mark Diamond Research Fund

Mark Diamond Research Fund

  • calandra-battersby
  • 0 Slides

Grant-Writing Tutorial. part 3. . Maximum 3 page...

An Introduction to Human Subjects Research

An Introduction to Human Subjects Research

  • aaron
  • 0 Slides

Office of Research Policies, Compliance, and Comm...

Rare Diseases Clinical Research Network

Rare Diseases Clinical Research Network

  • lois-ondreau
  • 0 Slides

Data Management and Coordinating Center (RDCRN DM...

Leonard Ortmann Renee Ross

Leonard Ortmann Renee Ross

  • karlyn-bohler
  • 0 Slides

Natalie Brown. Betty Wong. Scientific Ethics and...

Ethics Today : Cases IRB Administrators 2012

Ethics Today : Cases IRB Administrators 2012

  • min-jolicoeur
  • 0 Slides

PRIDE:. Theresa Straut. , CIP, RAC. Lucindia Shou...

Research Study Documentation

Research Study Documentation

  • briana-ranney
  • 0 Slides

Good Intention is Not Enough!. If Robin Hood were...

Part 3 of 3 part series: Informed

Part 3 of 3 part series: Informed

  • danika-pritchard
  • 0 Slides

consent: . Documentation. Wendy Lloyd. BA, LPN,...

ORD Common Questions

ORD Common Questions

  • tawny-fly
  • 0 Slides

K. Lynn Cates, MD. Assistant Chief Research &...

Deception Research HRPP Coordinator Meeting

Deception Research HRPP Coordinator Meeting

  • faustina-dinatale
  • 0 Slides

May 19, 2017. What is Deception?. Deception is wh...

Study Start-Up and Implementation

Study Start-Up and Implementation

  • mitsue-stanley
  • 0 Slides

PEARLS December 9, 2016. Panelists. Saadia Khizer...

Julie Bouma, Jacob Holloway and Cathy Peterson

Julie Bouma, Jacob Holloway and Cathy Peterson

  • danika-pritchard
  • 0 Slides

WMed HRPP . Investigator Responsibilities for . C...

Understanding Data Registry Setup and Maintenance

Understanding Data Registry Setup and Maintenance

  • alexa-scheidler
  • 0 Slides

Policies. Nichole Haywood. IRB Protocol Analyst. ...

Sponsor Expectations for Clinical Studies

Sponsor Expectations for Clinical Studies

  • marina-yarberry
  • 0 Slides

Stephen Workman, MPH. September 2016. Thomas Jeff...

Deception’s Second Cousin:

Deception’s Second Cousin:

  • test
  • 0 Slides

Participant Observation. IRB Continuing Education...

Human subjects research Session 1:

Human subjects research Session 1:

  • olivia-moreira
  • 0 Slides

Basic hhs and nih requirements. Yvonne lau – Of...

Lee Ann Hawkins, PhD. RN, FNP-BC

Lee Ann Hawkins, PhD. RN, FNP-BC

  • myesha-ticknor
  • 0 Slides

Assistant Professor . Division of Graduate Studie...

C onflict of I nterest

C onflict of I nterest

  • alida-meadow
  • 0 Slides

for Institutional Review Boards. Jane Gutcher. Of...

Re-Consent or Notification of Significant New Findings Developed During the Course of Research

Re-Consent or Notification of Significant New Findings Developed During the Course of Research

  • pasty-toler
  • 0 Slides

When will You need to ‘re-Consent’ Study Subj...

HawkIRB Research TEAM IRB Training May 2014

HawkIRB Research TEAM IRB Training May 2014

  • ellena-manuel
  • 0 Slides

Michele . Myrvik. Program Specialist. Research &a...

ORO Findings on Privacy, Confidentiality, and Information Security

ORO Findings on Privacy, Confidentiality, and Information Security

  • ellena-manuel
  • 0 Slides

Peter N. Poon, JD, MA, . CIPP. /G. Office of Rese...

Preparing for an FDA Inspection

Preparing for an FDA Inspection

  • tawny-fly
  • 0 Slides

. Kathy Gilmartin, MSN, CRN...

1 Developed by: U-MIC To start the presentation, click on this button in the lower right corner of

1 Developed by: U-MIC To start the presentation, click on this button in the lower right corner of

  • myesha-ticknor
  • 0 Slides

enter. .. IRB Board meeting minutes. Developed by...

Informed Consent UTHSC Institutional Review Board (IRB)

Informed Consent UTHSC Institutional Review Board (IRB)

  • marina-yarberry
  • 0 Slides

Session Overview. Process and Documentation. Vuln...

Culminating Experience updated 9/24/14

Culminating Experience updated 9/24/14

  • pamella-moone
  • 0 Slides

Department . of Prevention and Community Health. ...

Preparing for an FDA Inspection

Preparing for an FDA Inspection

  • min-jolicoeur
  • 0 Slides

. Kathy Gilmartin, MSN, CRN...

SO YOU THINK YOU WANT TO DO RESEARCH, HUH?

SO YOU THINK YOU WANT TO DO RESEARCH, HUH?

  • jane-oiler
  • 0 Slides

Laura Herbelin, Research Instructor. University o...

Tool: Training Presentation: Investigator Responsibilities and Good Clinical Practice (GCP)

Tool: Training Presentation: Investigator Responsibilities and Good Clinical Practice (GCP)

  • ellena-manuel
  • 0 Slides

Based on ICH . E6. GCP Guidance (. Sections1.24....

Expedited Reporting Darlene Kitterman,

Expedited Reporting Darlene Kitterman,

  • jane-oiler
  • 0 Slides

MBA. Director, Investigator Support & Integra...

Common Problems in Informed Consent

Common Problems in Informed Consent

  • jane-oiler
  • 0 Slides

Jeri R. . Barney. , JD, . MS . . Michele . Ant...

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