Serious Adverse events & SAE reporting - With SUGAM Portal Updates on SAE submission
Рет қаралды 4,739
Күн бұрынIn this video, I explain Serious Adverse Events (SAE) in clinical trials and all the criteria for SAE. We also talk about SAE reporting timelines and submissions. The latest SUGAM portal updates for SAE reporting & submission are also provided to stay updated on latest development and regulatory requirements
(0:00) Intro
(0:37) What are Serious Adverse events?
(2:03) Criteria for SAE
(4:10) Impact of SAE on Clinical Trials
(5:34) SAE Reporting and SAE Timelines
(8:13) New SAE Reporting on SUGAM Portal
(10:16) 24 hr SAE Reporting on SUGAM Portal
(12:00) 14 Days SAE Reporting on SUGAM Portal
For any queries, kindly mention in the description box below.
@amitjoshi1138 Жыл бұрын
Thank you sir ☺️
@harshamani7722 3 жыл бұрын
Nyc video sir...plzz make a video on drug regulatory affairs
@dileepkushwaha5789 Жыл бұрын
Very helpful vidio sir
@sheetalkasbe6842 3 жыл бұрын
Please make more videos regarding management of Adverse drug reaction and terminologies of ADR
@mklsa7548 3 жыл бұрын
A friend of mine recommend ur channel... & To be very honest Bhut shi videos banate ho yr... Is their any way to reach u out... Meri bhut queries hai SAS Ko lkr... & Abhie Clinical SAS sikh rha hoon isliye... 🙏🙏🙏 😀
@dubbakaaravind286 3 жыл бұрын
Hi sir.. Can u plz make a interview of clinical SAS programmer regarding jobs and best coaching centre in Hyderabad...
@swagatikapanda6895 3 жыл бұрын
Please upload some videos on real time sas programmer work....
@shaikmahaboobbasha318 3 жыл бұрын
Please tell me the forms used to fill the sae report
@mklsa7548 3 жыл бұрын
Hi, could u please tell me something about banking domain, what kind of real cases that a sas developer performs in that domain...
@clinicalresearchx360 3 жыл бұрын
Mostly business analytics and statistics trends and financial projections based on it particularly for the banking domain
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