'Irb approval' presentation slideshows

HIPAA Privacy Rule

HIPAA Privacy Rule. Paul Below Clinical Research Consultant . Training Objectives. Overview of the HIPAA Privacy Rule and its impact on clinical research Quiz. Disclaimer / Disclosure.

838 views • 55 slides

Clinical Research in the Emergency Department

Clinical Research in the Emergency Department. Jim Quinn MD MS Associate Professor of Surgery/Emergency Medicine Research Director Emergency Medicine. Overview. Goals for research in academic emergency medicine Problems/solutions for researchers in emergency medicine

780 views • 54 slides

Part 2 of 3 part series: Informed consent: The Process

Part 2 of 3 part series: Informed consent: The Process. Wendy Lloyd BA, LPN , CIP,CCRP Regulatory Affairs and Compliance Specialist. Objectives. Identify consent process requirements Distinguish between IRB, PI/Designee consent process responsibilities

706 views • 52 slides

Kimberly Summers, PharmD Deputy ACOS for Research South Texas Veterans Health Care System

VA Research: IRB and R&D Approval Process From Initial Submission, Through the Informed Consent Process and Continuing Review, To Inactivation. Kimberly Summers, PharmD Deputy ACOS for Research South Texas Veterans Health Care System Research & Development Service. Overview.

619 views • 46 slides

Shahrokh F. Shariat , MD Chair and Professor, Medical University of Vienna, Vienna, AUT

Clinical research original article: How to write an article and get it published in European Urology. Shahrokh F. Shariat , MD Chair and Professor, Medical University of Vienna, Vienna, AUT

621 views • 46 slides

The Institutional Review Board (IRB) and its functions

The Institutional Review Board (IRB) and its functions. Anthony K. Wutoh, Ph.D., R.Ph. Chairman & Professor School of Pharmacy College of Pharmacy, Nursing and Allied Health Sciences. Howard University IRB. What is your image of the IRB?. Who can we frustrate today ?.

599 views • 41 slides

Florida Clinical Laboratory Cancer Identification Program (CLIP)

Florida Clinical Laboratory Cancer Identification Program (CLIP). FCDS 2002 Educational Teleconference Series http://fcds.med.miami.edu Steven Peace, CTR Mayra Alvarez, RHIT, CTR June 26, 2002. CLIP Program Announcements. February 8, 2002 - Program Announcement

817 views • 37 slides

Investigational Device Exemptions 21 CFR Part 812

A Review for OCRA US RAC Study Group September 2005 Ginger Clasby, MS Promedica International gclasby@promedica-intl.com 714-799-1617 x 25. Investigational Device Exemptions 21 CFR Part 812. IDE About the Regulation.

619 views • 30 slides

man Research Protections and Quality Assurance

man Research Protections and Quality Assurance Institutional Review Board Orientation & IRB Submission Process Kevin Nellis, MS, CIP Executive Director, Human Research Protections and Quality Assurance. Institutional Review Board (IRB ) & Privacy Board.

456 views • 27 slides

Designing Experiments

Designing Experiments. Lorrie Faith Cranor September 2009. How is HCISEC different from HCI?. Is it different? If so, how? Are different user study methods needed?. Designing and conducting a user study. Identify purpose and metrics Decide what type of data to collect Design tasks

415 views • 22 slides

Crowdsourcing pharmacogenomic data analysis: PGRN-Sage RA Responder Challenge

358 views • 22 slides

Chapter 15: Narrative Research

Chapter 15: Narrative Research. Objectives Briefly state the definition and purpose of narrative research and describe the narrative research process.

5.42k views • 21 slides

Current IRB at DMACC

Current IRB at DMACC. September 2018. General Types of Human Research. RESEARCH that involves direct interaction with individuals (e.g., in person, or via mail, email, web survey, or telephone), or data from human subjects for which the researchers will have access to identifiers.

326 views • 18 slides

Navigating the IRB process

254 views • 17 slides

Conflict and Consent: Managing Disclosure in Human Subjects Research

Conflict and Consent: Managing Disclosure in Human Subjects Research. University of Miami Human Subjects Research Office Conflict of Interest Symposium May 11, 2007 Kenneth W. Goodman, Ph.D. University of Miami Ethics Programs kgoodman@miami.edu. Context. Ethics precedes regulation

399 views • 16 slides

Teaching Research Methods (Classroom Protocols)

435 views • 15 slides

Genomic Medicine Pilot Demonstration Projects

National Human Genome Research Institute. Genomic Medicine Pilot Demonstration Projects. U.S. Department of Health and Human Services National Institutes of Health National Human Genome Research Institute. National Institutes of Health. Teri Manolio, M.D., Ph.D.

313 views • 15 slides

Using an On-line Survey Tool to Streamline Outcomes Assessment

Using an On-line Survey Tool to Streamline Outcomes Assessment. Phillip R. Rosenkrantz, Ed.D., P.E. Industrial & Manufacturing Engineering Department California State University, Pomona. Topics. Introduction Examples of Survey Use Design & Deployment Features Analysis & Sharing Features

239 views • 15 slides

60 Second Science: Presentations by CPHI Pilot Grant Recipients

454 views • 14 slides

Breakthrough Technology for a Brighter Future

Breakthrough Technology for a Brighter Future . Oramed Pharmaceuticals. OTC Bulletin Board: ORMP Company with oral drug delivery platform Based on over 25 years of medical research at Hadassah University Medical Center - Jerusalem World leading scientific team Experienced management team

357 views • 10 slides