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