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Search Results for 'Hinu Irb'

Hinu Irb published presentations and documents on DocSlides.

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...

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...

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