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GW OHR IRB
เข้าร่วมเมื่อ 26 ส.ค. 2015
IRB PROCESS
IRB Process
The IRB staff will lead you through the submission process. Learn about the regulatory review process including categories of review and what the IRB looks for in the criteria of approval. Breakout sessions for students and investigators will be hosted by IRB staff.
Target Audience: ALL RESEARCHERS that conduct biomedical research, social behavioral research, or a combination of the two.
The IRB staff will lead you through the submission process. Learn about the regulatory review process including categories of review and what the IRB looks for in the criteria of approval. Breakout sessions for students and investigators will be hosted by IRB staff.
Target Audience: ALL RESEARCHERS that conduct biomedical research, social behavioral research, or a combination of the two.
มุมมอง: 5 888
วีดีโอ
IRB PANEL DISCUSSION
มุมมอง 4548 ปีที่แล้ว
International Research Panel Discussion Join seasoned researchers as they discuss the challenges and barriers to conducting research in an international setting. The panelist include Dr. Kate Applebaum, Milken Institution School of Public Health; Dr. David Diemert, School of Medicine and Health Sciences; and Dr. Jim Williams, Graduate School of Education and Human Development and the Elliot Sch...
Good Clinical Practice
มุมมอง 41K8 ปีที่แล้ว
Coordinator/Investigator Training: Good Clinical Practice The afternoon session will cover Good Clinical Practice in a research setting. This session is ideal for all coordinators and investigators. *ACRP Continuing Education Credits will be offered for the September 15 sessions. These credits may be applied for re-certification of CCRC or CCRA credentials. Target Audience: All Coordinators and...
2015 Fall IRB Days 9/15 AM Session: Human Subject Regulations 1
มุมมอง 1.9K8 ปีที่แล้ว
Coordinator/Investigator Training: OHRP and FDA regulations and Guidance This morning session will focus on regulations both for Office for Human Research Protections and the Food and Drug Administration. We will cover regulations, conduct case study analyses of regulation violations and provide information on how to prepare for an audit. *ACRP Continuing Education Credits will be offered for t...
June 2015 IRB Forum International Research 1
มุมมอง 1318 ปีที่แล้ว
June 2015 IRB Forum International Research 1
Research Seminar Series 4 Office of Human Research Ross 101, 4 16 2014, 12pm
มุมมอง 1248 ปีที่แล้ว
Research Seminar Series 4 Office of Human Research Ross 101, 4 16 2014, 12pm
A quick question please.If a particpant makes an error on the ICF ,are they supposed to correct it using the GCP guidelines considering they are not required to be GCP compliant ?
One the best video about clinical research ! Thanks for sharing
The source documents section includes IRB approvals; wouldn’t this be essential documents kept in the regulatory binder!?
Thanks for sharing this information watching from Ghana I love this program
Thanks for sharing :) 🙏
many thanks .it was really useful
This vid is so so cool! I've been trying to search for a video similar to yours that really informs everything in this TH-cam video! 🧑⚕️Your explanation totally reminds me of the videos from this new Doctor Ethan! His videos are for sure insightful and I learned a lot for finals! He is an informative Dr! Go check his page out and give Dr Ethan a subscribe here! ➡️ #DoctorEthanMedLife
Hi all, I believe on slide two, it should be 21CFR Part 11, not part 111.
I agree.
Beyond alarming.
Is everything in this video highly applicable in a clinical trial setting as well? Great video!
Very helpful and informative. Please keep loading these lectures. Thank you.
thank you for help us by useful information very interesting lecture .
Thanks so much ....thanks for the clear elaboration!...nice lecture!!
thank you so much for sharing 😊 great lecture