Good Clinical Practice

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 Investigators

[@HaMou261]

One the best video about clinical research ! Thanks for sharing

[@natybixcoito01]

thank you so much for sharing 😊 great lecture

[@jumaarbab1343]

thank you for help us by useful information very interesting lecture .

[@RepampGhana]

Thanks for sharing this information watching from Ghana I love this program

[@yanetcruz9069]

Very helpful and informative. Please keep loading these lectures. Thank you.

[@healthtrackers]

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 ?

[@eunkyochoi2238]

Thanks for sharing :) 🙏

[@nejatmuhammady9840]

many thanks .it was really useful

[@kevintran1156]

Is everything in this video highly applicable in a clinical trial setting as well? Great video!

[@lilianmayieka9676]

Thanks so much ....thanks for the clear elaboration!...nice lecture!!

[@sptzk7133]

The source documents section includes IRB approvals; wouldn’t this be essential documents kept in the regulatory binder!?

[@Jean3claude]

Hi all, I believe on slide two, it should be 21CFR Part 11, not part 111.

[@wrongfulconvictions1]

I agree.