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Irb-Cloud published presentations and documents on DocSlides.

ORD Common Questions
ORD Common Questions
by tawny-fly
K. Lynn Cates, MD. Assistant Chief Research &...
Deception Research HRPP Coordinator Meeting
Deception Research HRPP Coordinator Meeting
by faustina-dinatale
May 19, 2017. What is Deception?. Deception is wh...
Part 3 of 3 part series: Informed
Part 3 of 3 part series: Informed
by danika-pritchard
consent: . Documentation. Wendy Lloyd. BA, LPN,...
Research Study Documentation
Research Study Documentation
by briana-ranney
Good Intention is Not Enough!. If Robin Hood were...
Ethics Today : Cases IRB Administrators 2012
Ethics Today : Cases IRB Administrators 2012
by min-jolicoeur
PRIDE:. Theresa Straut. , CIP, RAC. Lucindia Shou...
Leonard Ortmann Renee Ross
Leonard Ortmann Renee Ross
by karlyn-bohler
Natalie Brown. Betty Wong. Scientific Ethics and...
An Introduction to Human Subjects Research
An Introduction to Human Subjects Research
by aaron
Office of Research Policies, Compliance, and Comm...
Rare Diseases Clinical Research Network
Rare Diseases Clinical Research Network
by lois-ondreau
Data Management and Coordinating Center (RDCRN DM...
Mark Diamond Research Fund
Mark Diamond Research Fund
by calandra-battersby
Grant-Writing Tutorial. part 3. . Maximum 3 page...
Preparing for your Research
Preparing for your Research
by jane-oiler
Project. Christopher Kabir, MS. PCOR Coordinator....
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
by pasty-toler
Submitting an Amendment. Step 1: Log into IRBMana...
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by danika-pritchard
University of Kentucky E-IRB. Application Feature...
cHildren’s Findings An IRB
cHildren’s Findings An IRB
by cheryl-pisano
Infoshort. November . 2012.
© HRP Consulting Group Investigator Responsibilities in Human Subjects Research
© HRP Consulting Group Investigator Responsibilities in Human Subjects Research
by liane-varnes
Jeffrey M. Cohen, Ph.D. CIP. Chief Executive Offi...
1 Updating the Common Rule Governing Human Subjects Research Protections
1 Updating the Common Rule Governing Human Subjects Research Protections
by tawny-fly
Jerry Menikoff. 2. 2. Disclaimer. The views expr...
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;
by test
2. Highlight specific questions to ask when dete...
UC DIG REF CONFERENCE CALL
UC DIG REF CONFERENCE CALL
by pamella-moone
AGENDA. Monday March 30, 2015 . 1. .) . Reporting...
ROAD MAP: Getting a Cancer Study Done at Jefferson
ROAD MAP: Getting a Cancer Study Done at Jefferson
by ellena-manuel
Sylvia O’Neill, MD. Associate Director of Regul...
Stony Brook University
Stony Brook University
by tatyana-admore
The Process for Joining TIES. Project Team:. PI ...
Good Clinical Practices
Good Clinical Practices
by pamella-moone
Presented By :. Version: 1.0/2017. 1. Good clinic...
Honest Brokers for Secure De-identification of Patient Reco
Honest Brokers for Secure De-identification of Patient Reco
by stefany-barnette
Project – CSE 5810 – Introduction to Biomedic...
Monday February 9, 2015  2/9/15
Monday February 9, 2015  2/9/15
by ellena-manuel
Today's Agenda. D. ue Dates. Pass In Open Mind Ac...
Dartmouth Human Research Protection Program (HRPP)
Dartmouth Human Research Protection Program (HRPP)
by danika-pritchard
Brown Bag Series: First Tuesday of the Month. The...
The Nuremberg
The Nuremberg
by faustina-dinatale
Code 1947. Rels. 300 / . Nurs. 330. 22 October ...
SITE CLOSEOUT – AN OVERVIEW
SITE CLOSEOUT – AN OVERVIEW
by stefany-barnette
Presented by:. Maria Campanella, BSN, RN, CCRA. M...
Evaluation and Human Subjects Research
Evaluation and Human Subjects Research
by ellena-manuel
Julie M. Aultman, Ph.D.. Chair, Institutional Rev...
Project Completion Report
Project Completion Report
by natalia-silvester
ESTR Product Path Project. April 2016 . Presentat...
Ethical Considerations When Designing and Conducting Intern
Ethical Considerations When Designing and Conducting Intern
by tawny-fly
CTE. DCS IRB Series – Event 3. December 1,2014....
San Francisco
San Francisco
by conchita-marotz
Department of Public Health . SPNS Grantee Meeti...
Approval Criteria – Informed Consent
Approval Criteria – Informed Consent
by calandra-battersby
Angela Bain, . IRB Administrator. abain@uga.edu. ...
Institutional Review Board
Institutional Review Board
by pamella-moone
History and Ethics. 2. Ethical History. 1939-1945...
A ROMP in the PARC: Research on Medical Practices--Patient
A ROMP in the PARC: Research on Medical Practices--Patient
by luanne-stotts
David Magnus, PhD. Thomas A. Raffin Professor of ...
Navigating Non-Compliance
Navigating Non-Compliance
by yoshiko-marsland
Angela Bain, . IRB Administrator. abain@uga.edu. ...
Beach Patrol Framework
Beach Patrol Framework
by ellena-manuel
Core Values. Uniformity for Controlled Quality As...
HIPAA Privacy Rule and Research
HIPAA Privacy Rule and Research
by cheryl-pisano
Kaiser Permanente Researcher Training. Marc...
Biomedical Informatics
Biomedical Informatics
by debby-jeon
Update and Tools. Arthur Berg, PhD. Bioinformatic...
Levels of Review
Levels of Review
by trish-goza
West Virginia University. Office of Research Inte...
Transition to email IRB submissions
Transition to email IRB submissions
by danika-pritchard
Informational session. * . To play . The...
What is exempt research?
What is exempt research?
by stefany-barnette
Angela Bain, . IRB Administrator. abain@uga.edu. ...
Ineligible Subjects: Common Causes, and Tips for Prevention
Ineligible Subjects: Common Causes, and Tips for Prevention
by olivia-moreira
Jess Randall, MA, . CIP, Compliance Manager. Jeri...