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Irb Student published presentations and documents on DocSlides.

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...

Did that just happen? And

Did that just happen? And

  • mitsue-stanley
  • 0 Slides

What do I do now?. Identifying and Reporting . A...

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...

CARA Moose Mountain Sept 2011 VHF Contest Expedition

CARA Moose Mountain Sept 2011 VHF Contest Expedition

  • trish-goza
  • 42 Slides

CARA Moose Mountain Sept 2011 VH...

CARA Moose Mountain Sept 2011 VHF Contest Expedition

CARA Moose Mountain Sept 2011 VHF Contest Expedition

  • kittie-lecroy
  • 42 Slides

CARA Moose Mountain Sept 2011 VH...

1 King & Spalding May 22, 2014

1 King & Spalding May 22, 2014

  • marina-yarberry
  • 60 Slides

1 King & Spalding ...

UC DAVIS OFFICE OF RESEARCH

UC DAVIS OFFICE OF RESEARCH

  • olivia-moreira
  • 27 Slides

Overview of Good Clinical Practices (GCP) . Inves...

Research Ethics & Integrity

Research Ethics & Integrity

  • eurolsin
  • 28 Slides

Susan L. Rose, Ph.D.. Office for the Protection of...

Overview of the Office Of Research Assurances (ORA)

Overview of the Office Of Research Assurances (ORA)

  • bitechmu
  • 39 Slides

Office of Research Assurances. 205 . Albrook. , Pu...

Guide To Collaborative Institutional Training Initiative (CITI) Program

Guide To Collaborative Institutional Training Initiative (CITI) Program

  • mjnt
  • 23 Slides

Tennessee . State University . Institutional . Rev...

Task Order Activities Study Status

Task Order Activities Study Status

  • dayspiracy
  • 2 Slides

(IRB status). TO #8: MDR-TB Genotyping. Patient in...

Good Clinical Practices Marianne Kearney Chase

Good Clinical Practices Marianne Kearney Chase

  • jubilantbikers
  • 47 Slides

Director of Research Operations. Neurological Clin...

SEND 2.0 Sofija Konjević, sofija@irb.hr

SEND 2.0 Sofija Konjević, sofija@irb.hr

  • blackwidownissan
  • 9 Slides

Bojan Macan, bmacan@irb.hr. Novo ruho međuknjižn...

Research Compliance: Protections for Research Subjects

Research Compliance: Protections for Research Subjects

  • easyho
  • 16 Slides

NMU Graduate Education and Research. September 201...

Podučavanje korisnika Iskustva Knjižnice IRB-a

Podučavanje korisnika Iskustva Knjižnice IRB-a

  • markes
  • 9 Slides

Bojan Macan, viši knjižničar. Knjižnica Instit...

Sponsor-Investigator (SI) FDA Inspections

Sponsor-Investigator (SI) FDA Inspections

  • eurolsin
  • 11 Slides

Christiana Provencal, M.A.. Quality Assurance / Qu...

Corrective and Preventative Action Plans (CAPAs)

Corrective and Preventative Action Plans (CAPAs)

  • imetant
  • 16 Slides

Common Pitfalls and Solutions. Human Research Prot...

ABB ROBOTICSYuMiIRB 14000Overview

ABB ROBOTICSYuMiIRB 14000Overview

  • jalin
  • 29 Slides

— — — Overview and vision Technical...

Revised Common Rule: Informed Consent

Revised Common Rule: Informed Consent

  • mia
  • 58 Slides

Content, Documentation, Broad Consent, and Posting...

By Certified

By Certified

  • udeline
  • 5 Slides

Mail - 5 and 2001, Ms. Karen M. Kondas and Mr. S...

VeloseIRB Study Registration

VeloseIRB Study Registration

  • felicity
  • 12 Slides

1Page 1Velosis a study management tool used to hel...

UNIVERSITY OF CALIFORNIA SAN DIEGOHUMAN RESEARCH PROTECTIONS PROGRAMHu

UNIVERSITY OF CALIFORNIA SAN DIEGOHUMAN RESEARCH PROTECTIONS PROGRAMHu

  • eleanor
  • 4 Slides

Some researchers may have already completed the CI...

PROTECTED A SECURITY when Completed

PROTECTED A SECURITY when Completed

  • sophia
  • 21 Slides

nformation echnologySecurity RequirementsHandling ...

NSTRUCTION321602ROTECTION OF UMAN UBJECTS AND DHERENCE TO THICAL TANDA

NSTRUCTION321602ROTECTION OF UMAN UBJECTS AND DHERENCE TO THICAL TANDA

  • lily
  • 35 Slides

Originating ComponentOffice of the Under Secretary...

Preparing for an FDA Inspection

Preparing for an FDA Inspection

  • felicity
  • 49 Slides

. Kathy Gilmartin, MSN, CRNP, CCRC. ...

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

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

  • samantha
  • 47 Slides

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

Considerations for IRB Review of Cell-Based Therapies

Considerations for IRB Review of Cell-Based Therapies

  • paige
  • 10 Slides

D. Craig Hooper, PhD, FNAI. Professor of Cancer ...

Speaking Clinical Trials

Speaking Clinical Trials

  • ruby
  • 48 Slides

Marianne Kearney. Director of Research Operations ...

Responsibilities of the Principal Investigator

Responsibilities of the Principal Investigator

  • faith
  • 36 Slides

Anne Roussell, RN. [adapted from . MAGI/. Complion...

The Fundamentals of Clinical Research

The Fundamentals of Clinical Research

  • harper
  • 59 Slides

Prepared by Christine Hunter, BSN Baylor College ...

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