One the best video about clinical research ! Thanks for sharing
@RepampGhana
2 жыл бұрын
Thanks for sharing this information watching from Ghana I love this program
@yanetcruz9069
6 жыл бұрын
Very helpful and informative. Please keep loading these lectures. Thank you.
@jumaarbab1343
7 жыл бұрын
thank you for help us by useful information very interesting lecture .
@natybixcoito01
8 жыл бұрын
thank you so much for sharing 😊 great lecture
@nejatmuhammady9840
2 жыл бұрын
many thanks .it was really useful
@eunkyochoi2238
2 жыл бұрын
Thanks for sharing :) 🙏
@sptzk7133
2 жыл бұрын
The source documents section includes IRB approvals; wouldn’t this be essential documents kept in the regulatory binder!?
@Jean3claude
3 жыл бұрын
Hi all, I believe on slide two, it should be 21CFR Part 11, not part 111.
@wrongfulconvictions1
3 жыл бұрын
I agree.
@healthtrackers
Жыл бұрын
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 ?
@lilianmayieka9676
8 жыл бұрын
Thanks so much ....thanks for the clear elaboration!...nice lecture!!
@kevintran1156
6 жыл бұрын
Is everything in this video highly applicable in a clinical trial setting as well? Great video!
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