One the best video about clinical research ! Thanks for sharing
@RepampGhana2 жыл бұрын
Thanks for sharing this information watching from Ghana I love this program
@jumaarbab13437 жыл бұрын
thank you for help us by useful information very interesting lecture .
@yanetcruz90697 жыл бұрын
Very helpful and informative. Please keep loading these lectures. Thank you.
@nejatmuhammady98402 жыл бұрын
many thanks .it was really useful
@natybixcoito018 жыл бұрын
thank you so much for sharing 😊 great lecture
@eunkyochoi22382 жыл бұрын
Thanks for sharing :) 🙏
@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 ?
@sptzk71332 жыл бұрын
The source documents section includes IRB approvals; wouldn’t this be essential documents kept in the regulatory binder!?
@Jean3claude4 жыл бұрын
Hi all, I believe on slide two, it should be 21CFR Part 11, not part 111.
@wrongfulconvictions13 жыл бұрын
I agree.
@kevintran11566 жыл бұрын
Is everything in this video highly applicable in a clinical trial setting as well? Great video!
@lilianmayieka96768 жыл бұрын
Thanks so much ....thanks for the clear elaboration!...nice lecture!!