ฝัง
- เผยแพร่เมื่อ 25 ก.ค. 2018
- Regulatory Documents For Clinical Research Sites Webinar
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The best cllinical research webinar on regulatory requirements for SSU that I've seen. Thank you!
Awesome! Thanks
Great webinar! A lot of useful knowledge with the eye of practitioner.
awesome as always, am so lucky to have found this webinar. First and foremost can you be kind enough to share these slides? Secondly, in relation to the financial disclosure slide, if there is no IP hence no pharmaceutical company, do we forego this disclosure since it says ..."no financial interest in the pharmaceutical company conducting the study" ? or is the sentence then just modified to the type of study? i hope I am making sense, I am from Zambia English is not native and am new to research at this level, just left clinical practice. Thanks
concerning IRB approval, even if the site has no ongoing study in that particular year should they still have a yearly renewed approval or this is done just with receipt of a study?
concerning credentials, as we file renewed licenses, how far back can we continue to keep expired licenses on file or can we discard?
some serious stuff..goodnight
Chris had a point behind the kidding statement, log makes sense,but P.I should act sensibly and be knowledgeable, of course for the benefit of the patients without co intervention/ deviation from protocol😇
Nice job guys
thank you!
Please help me to understand initial crucial documents require to start study
Thanks for this webinar, it is very informative. please where can I get GCP training certification...which institution/site offers the certification training?? Thank you..
thank you dan for the excllent video , is study start up just in phase 1 or all single phase we do same steps and documents ?
Any study
Basic things in the forms on all countries are the same.
I have a bs in science 2012 , i also have phlebotomist certification, i want get in field, what more certification or skills i need to get in field
just start at a research clinic near you
Is this applicable for the uk
Yes
Difference between SUSARA and CIOMA?
Dont know what cioma is
Do all subjects start on same date.....for example for a Phase 2 trial of may be 10 to 20 Subjects .....are they all starting same day upon Site Initiation
No. Subjects can start whenever they can. Sites cannot screen any until after siv. Know the difference between enrollment window and study duration
@@dansfera just saw this clip.....www.theclinicaltrialsguru.com/blog1/enrollment-window-vs-study-length-in-clinical-trials
@@dansfera can I have your mobile number or email address