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Search Results for 'Unanticipated Irb'

Unanticipated Irb published presentations and documents on DocSlides.

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...

C onflict of I nterest

C onflict of I nterest

  • marina-yarberry
  • 0 Slides

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

Overview of the Office of Research

Overview of the Office of Research

  • liane-varnes
  • 0 Slides

Assurances (ORA). Office of Research Assurances. ...

Checklist for reviewing Privacy, Confidentiality

Checklist for reviewing Privacy, Confidentiality

  • cheryl-pisano
  • 0 Slides

and Information Security. in Research. VA OI&...

Good Clinical Practice (GCP) and Monitoring Practices

Good Clinical Practice (GCP) and Monitoring Practices

  • karlyn-bohler
  • 0 Slides

Office of Human Subjects Research Institutional R...

Social and Behavioral Science in Medical Research

Social and Behavioral Science in Medical Research

  • liane-varnes
  • 0 Slides

Judy Birk, JD . IRBMED Director. Cindy Shindledec...

Safety of the Subject Cena Jones-Bitterman, MPP, CIP, CCRP

Safety of the Subject Cena Jones-Bitterman, MPP, CIP, CCRP

  • natalia-silvester
  • 0 Slides

Holden Comprehensive Cancer Center. Protocol Deve...

Orientation for New Clinical Research PERSONNEL

Orientation for New Clinical Research PERSONNEL

  • lindy-dunigan
  • 0 Slides

Module 2. Presented by . NC TraCS Institute. UNC ...

Revised Common Rule: Informed Consent

Revised Common Rule: Informed Consent

  • danika-pritchard
  • 0 Slides

Content, Documentation, Broad Consent, and Postin...

Good Clinical Practices Presented By :

Good Clinical Practices Presented By :

  • stefany-barnette
  • 0 Slides

Version: 1.0/2017. 1. Good clinical Practices. Go...

Trial Innovation Network

Trial Innovation Network

  • sherrill-nordquist
  • 0 Slides

Network. Capacity. Thomas Flaig, MD. Director of...

How to Change the Principal Investigator (PI) in IRBNet and the Part I cover

How to Change the Principal Investigator (PI) in IRBNet and the Part I cover

  • faustina-dinatale
  • 5 Slides

How to Change the Principal Investigator (PI) in...

Orientation for New Clinical Research PERSONNEL Module 2 Presented by

Orientation for New Clinical Research PERSONNEL Module 2 Presented by

  • test
  • 80 Slides

Orientation for New Clinical Research PERSONNEL M...

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