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Varooni Panchal
India
Приєднався 7 жов 2012
Actual Treatment (TRTA) vs Planned Treatment (TRTP)
Actual Treatment (TRTA) vs Planned Treatment (TRTP)
Переглядів: 19
Відео
ADaM Interview Technical Questions Set 15
Переглядів 3519 годин тому
Please note: Answers will be provided by the end of Year 2025 i.e. on Dec 2025. Best of Luck !!
SDTM Interview Technical Questions Set 14
Переглядів 54День тому
Please note: Answers will be provided by the end of Year 2025 i.e. on Dec 2025. Best of Luck !!
Traceability of Data in Clinical Trials
Переглядів 2814 днів тому
Traceability of Data in Clinical Trials
SAS Programmer vs Statistical Programmer
Переглядів 4921 день тому
SAS Programmer vs Statistical Programmer
Clinical Study Report (CSR) vs Case Report Form (CRF)
Переглядів 67Місяць тому
Clinical Study Report (CSR) vs Case Report Form (CRF)
Business Intelligence vs Business Analyst
Переглядів 13Місяць тому
Business Intelligence vs Business Analyst
Challenges from aCRF to Specifications
Переглядів 392 місяці тому
Challenges from aCRF to Specifications
Data Scientist vs Data Analyst vs Data Engineer vs Data Developer
Переглядів 922 місяці тому
Data Scientist vs Data Analyst vs Data Engineer vs Data Developer
2 - Clinical Trials Therapeutic Areas and Diseases
Переглядів 632 місяці тому
2 - Clinical Trials Therapeutic Areas and Diseases
1 - Efficacy Tables in Clinical Trials
Переглядів 1152 місяці тому
1 - Efficacy Tables in Clinical Trials
SAS Interview Technical Questions Set 13
Переглядів 613 місяці тому
SAS Interview Technical Questions Set 13
SAS Interview Technical Questions Set 12
Переглядів 543 місяці тому
SAS Interview Technical Questions Set 12
What are the answers ?
Answers will be provided by the end of Year 2025 i.e. on Dec 2025.
Kindly make a video on BIMO
Very good morning mam and thanks so much for making this video .
My Pleasure !! Glad it was helpful !! So nice of you !! Welcome !! Thanks for your feedback.
Hi mam Please make Tlfs scenario based interview questions
Very nice
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Is the deviation category and deviation type the same?
Please refer video scheduled on 19th Jan 2025 @ 5:00 PM Deviation Category vs Deviation Type -- ua-cam.com/video/-vxiZmJuJuI/v-deo.html
Mam kindly make video .how to understand tfls outputs .how to undertand the study by looking at the outputs by taking few tables in oncology to explain.please
Hi Mam please make a video for ADAM AND SDTM Interview Q and A.
Please refer video scheduled on 16th Jan 2025 @ 5:00 PM SDTM Interview Technical Questions Set 14 -- ua-cam.com/video/sU4_lIbG3jY/v-deo.html
Mam thank you so much once again for your greatest contribution
My Pleasure !! Glad it was helpful !! So nice of you !! Welcome !! Thanks for your feedback.
Hi Varooni, thank you for explanation. Can you please explain adurn and aduru calculation in months , weeks and years separately
Mam why we use planned dose for efficacy outputs.why can't we use the actual treatment .I mean TRTA vs TRAP
Please refer video scheduled on 23rd Jan 2025 @ 5:00 PM Actual Treatment (TRTA) vs Planned Treatment (TRTP) -- ua-cam.com/video/V3xGmlohp9Y/v-deo.html
Mam if possible make an video on traceability of data.how to do it .kindly explain.
Please refer video scheduled on 5th Jan 2025 @ 5:00 PM Traceability of Data in Clinical Trials -- ua-cam.com/video/uQ6aIizzzDQ/v-deo.html
Thanks so much madam .
My Pleasure !! Glad it was helpful !! So nice of you !! Welcome !! Thanks for your feedback.
Please explain the r program including clinical sas training
Is CSR and CRF is different mam. If they are different how ?
Please refer to Clinical Study Report (CSR) vs Case Report Form (CRF) -- ua-cam.com/video/MgTBPTzAJX4/v-deo.html
Thank you so much.
My Pleasure !! Glad it was helpful !! So nice of you !! Welcome !! Thanks for your feedback.
Madam thanks so much for your effort in making this video .
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Thank you so much for good video
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I am indebted for your knowledge sharing
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Mam your knowledge sharing is superb.thanks for sharing
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Thanks madam for bringing very important topic with well explanation 🎉🎉
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Nice presentation, i have one request madam, can you explain about efficacy tables
Please refer to Efficacy Tables in Clinical Trials -- ua-cam.com/video/u-4JWogTdVE/v-deo.html
Hello, maam, whats best number to contact you on whatsapp?
Please drop me an email on varooni.panchal@gmail.com stating the objective and purpose of discussion. I'll guide you accordingly. Thanks for asking !!
Well explained!
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Well explained!
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Well explained and easy to understand. Explained everything within 35 minutes. I appreciate your work!!
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Nicely explained
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Thanks for sharing
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What a nice topic. Well done.
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Extremely useful🙂
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Thanks a lot for making this video
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Thank you! It is very helpful to know the content of CSR
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Outstanding video
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mam may I know what app do you use for this voice in the video video?
Please refer to 5 Ways to Generate AI Voice | Clone -- ua-cam.com/video/_Vc8aoF9vxk/v-deo.html
Very nice and useful videos madam .but please use you own voice as previous videos
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Great tip!
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Thank you Varooni. Good content.
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Thank you very much mam for uploading very useful information, really wonderful explanation
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thank you so much Ms. Varooni to understand in a broader level. I have some questions would you mind to make me understand those. as far as my knowledge every successful study need to pass all 4 levels of clinical trials(I-Iv). in this life cycle where does the ISS and ISE occurs. and how to collect the multiple study data for a single NDA. Does it mean for every NDA the studies should occur in multiple level, and does the same sponsor will conduct all the studies or how. Please, explan.
My Pleasure !! Glad it was helpful !! So nice of you !! Welcome !! Thanks for your feedback. Welcome Sir !! Sure, I can answer your questions. Yes, that's correct every successful study need to pass all 4 levels of clinical trials phases ( I - IV ). ISS / ISE studies facilitate broad views of the investigational product’s overall efficacy and safety profiles. ISS / ISE are required by the USFDA as a critical component in NDA submission. The ISE and ISS are detailed integrated analyses of all relevant data from the clinical study reports that belong on Module 5 in the Electronic Common Technical Document Structure Defined by FDA. Sponsor evaluates, determines and decides which individual studies will be part of the NDA submission. You will understand better practically if you get opportunity to work on ISS / ISE studies. Only when you work practically on ISS / ISE studies all your questions will be answered automatically !!
Invaluable content, as always! Super helpful. Thank you!
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Thank you a lot, a real Treasure, would it be possible for you to share slide? Thanks again for the wealth of information.
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Thank you so much ma'am .ur videos helped me a lot. keep posting
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Thank you for so much for wonderful explanation. Is it possible to get this document or notes from you . Thanks in Advance !!
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Nice
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Can you provide the answers please?
Please refer to 2024 - SAS Technical Q&A Sets -- ua-cam.com/video/PCvmxqek6SY/v-deo.html
Best videos as always! Very succinct and easy to understand. Thank you! Tons of respect 🙏 biostatistician from the US
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Thanks Varooni ! its very helpful and I got all the necessary information which I required for ISS ISE submission.
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Wonderful explanation, thank you so much
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i used to think CROs only work on CDISC project
Thanks for your comment !! It's good to know you are now aware of non-CDISC projects as well.
Gm Mam, will you teach define xml and iss and ise pooled data?
Yes, will see define.xml in future and will inform all when it's video is ready. For the ISS & ISE Pooled Data I have already explained the structure and strategy for creating ISS & ISE pooled data in SAS Programming Challenges in ISS & ISE -- ua-cam.com/video/9MpYPVtaL00/v-deo.html I don't have any ISS & ISE Pooled data maybe you can create yourself dummy data and practice on it. !!