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clinical research sites and irb submissions
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clinical research sites and irb submissions
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Call/Text: (949) 415-6256
Follow Me On:
SnapChat: username is dansfera
0:06:08
clinical research sites and irb submissions
0:03:54
The Four Phases of Clinical Trials | Diversity in Clinical Trials | AKF
0:18:50
Walkthrough Of A Real Clinical Research IRB Initial Investigator Application Using CIRBI - For CRCs!
0:40:38
IRB and Clinical Trials
0:40:38
IRB and Clinical Trials
0:37:25
What Do Sites Report To IRBs and CRA Activities in Clinical Research
0:16:58
Foundations of Clinical Research
0:01:58
What Are IRBs In Clinical Research and Differences Between Central and Local IRBs
0:07:15
What Is In An IRB Initial Application Form That Clinical Research Coordinators Or CRAs Should Know?
0:06:45
How IRBs Protect Human Research Participants
0:02:18
Why Don't All Clinical Research Sites Get Compliant With Protocol Amendments At The Same Time?
0:01:09
Clinical Trials: The Role of the Principal Investigator, Sponsor, IRB and FDA.
0:53:05
What Brand New Clinical Research Sites Need To Know
0:38:44
Clinical Trials Toolkit Session: Western IRB Submission Training - Presented by Deena Horowitz
0:23:09
How To Get Clinical Trial Opportunities For Your Clinical Research Site
0:02:15
Clinical Research Fundamentals - Informed Consent and IRB Requirements
4:26:27
The Only Crash Course To Clinical Research You’ll Ever Need (full 5 hour OFFICIAL video)
1:11:45
Clinical Research Trials from Start to Finish
0:01:02
IRB and IEC in Clinical Research
0:01:53
When sponsors get irb approval and select sites for clinical trials
0:02:05
What is IRB?
1:01:14
Clinical Trials Overview: Phrases and Phases of a Clinical Trials
1:00:28
Regulatory Documents For Clinical Research Sites Webinar
0:05:33
Essential Documentation in Clinical Trials at Research Sites
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