Hi, this video has some related information on the difference between 'original' and 'standard' results.. The same is applicable for ranges as well. ua-cam.com/video/PhMb0Xh6xmY/v-deo.html. For example, if we get the blood glucose measured in local laboratory, they may report the unit in mg/dL and they provide the range which is considered in normal range in the same units of mg/dL. This is called original range. However, if you are asked to report the same glucose value in a unit of 'mmol/L' (which is considered standard) - you would convert the number which is reported in mg/dL to mmol/L by using an appropriate conversion factor. We need to do the same with the ranges as well. These range values in mmol/L are considred standard ranges. Hope this helps.
Hi VamsiKrishna. If I understand your question correctly, you mean to say that you only have aCRF and no programming specification for SDTM dataset creation, how to map (program SDTM dataset). Answer: There are no guidelines on this. In this case, programmer will have to search for the raw dataset and variable names and understand the transformation requirements and program for the dataset.
It depends.. for a simple table\listing it generally takes 4-5 hours. for a complex table\listing we may need 8-12 hours. Same goes for SDTMs and ADaM, simple datasets may need around 5-6 hours and complex ones may take 1-2 days. It also depends on the project's setup, state of data cleanliness, availability of standard macros, support on those macros etc.
@@mycsg sir it seems like you keep on writing codes...do you also get free time like you completed one table till the time you get next table , you relax for 2 3 days . Or no free time and keep on writing one after another codes. Pls share this as i am lazy coder and inbetween every work i need enough time and cant handle too much work pressure. Before switching to clinical sas good to get idea about work pressure.
It depends again.. A clinical programmer's job is not just writing back-to-back code. It also involves understanding the study design aspects, keeping up to date with industry standards, writing specifications, learning new programming techniques, working with validation programmers to resolve any mismatches, working with statisticians to clarify things, working with data management team to get data cleaned.. and much more.. If you are looking for a job that challenges you and rewards you, you will like being a clinical programmer. Hope this helps!
We are not sure if you have subscribed to our channel, this has been already uploaded. Below is the link for video related to timing variables. ua-cam.com/video/3s5VejgBjBk/v-deo.html
Your way of explanation just amazing!!
Thank you Witty1. Glad that you found it helpful.
I agree, It is very helpful. Thank you!!
very helpful pls keep posting more videos
Thanks for taking time to share your knowledge and educating new comers ❤
Thank you Mohan Krishna. Glad that you found this helpful. Sure, will continue to post more videos.
Amazing explanation thank you so much sir
You are most welcome
Thank you
You're welcome
Hello sir what's the difference between standard range and original range?
Hi, this video has some related information on the difference between 'original' and 'standard' results.. The same is applicable for ranges as well.
ua-cam.com/video/PhMb0Xh6xmY/v-deo.html.
For example, if we get the blood glucose measured in local laboratory, they may report the unit in mg/dL and they provide the range which is considered in normal range in the same units of mg/dL. This is called original range.
However, if you are asked to report the same glucose value in a unit of 'mmol/L' (which is considered standard) - you would convert the number which is reported in mg/dL to mmol/L by using an appropriate conversion factor. We need to do the same with the ranges as well. These range values in mmol/L are considred standard ranges. Hope this helps.
If we have only acrf for mapping program , then how to mapp, is there any guidens
Hi VamsiKrishna. If I understand your question correctly, you mean to say that you only have aCRF and no programming specification for SDTM dataset creation, how to map (program SDTM dataset).
Answer: There are no guidelines on this. In this case, programmer will have to search for the raw dataset and variable names and understand the transformation requirements and program for the dataset.
@@mycsg i am a programmer , in this organisation they have only acrf no specification excel. So I am not able to understand this
I suggest you discuss it with other more experienced programmers in your organization to understand the details.
Hi .. thanks for video... Can you please explain the standard result and normal value
Hi Arun, is this what you are looking for?
ua-cam.com/video/Dipj4jh5YIE/v-deo.html
Hi..Dude please can you make a video on how to do unit conversion in LB Domain?
Hi Somnath, I have created a similar post on the website. Hope it helps.
www.mycsg.in/posts_display.php?category=SDTM&uid=90
Tq sir it is more helpful
Always welcome
super explanation
Thank you Ravi Shankar. Glad that you found it helpful.
Sir How many tables/datasets you have to create in a day while working for a company....
It depends.. for a simple table\listing it generally takes 4-5 hours. for a complex table\listing we may need 8-12 hours. Same goes for SDTMs and ADaM, simple datasets may need around 5-6 hours and complex ones may take 1-2 days.
It also depends on the project's setup, state of data cleanliness, availability of standard macros, support on those macros etc.
@@mycsg sir it seems like you keep on writing codes...do you also get free time like you completed one table till the time you get next table , you relax for 2 3 days . Or no free time and keep on writing one after another codes. Pls share this as i am lazy coder and inbetween every work i need enough time and cant handle too much work pressure. Before switching to clinical sas good to get idea about work pressure.
Plz reply....
It depends again.. A clinical programmer's job is not just writing back-to-back code. It also involves understanding the study design aspects, keeping up to date with industry standards, writing specifications, learning new programming techniques, working with validation programmers to resolve any mismatches, working with statisticians to clarify things, working with data management team to get data cleaned.. and much more.. If you are looking for a job that challenges you and rewards you, you will like being a clinical programmer. Hope this helps!
Sir plz explain another variable like cmstnrf cmENRf and cmstrtpt and cmenrtpt
We are not sure if you have subscribed to our channel, this has been already uploaded. Below is the link for video related to timing variables.
ua-cam.com/video/3s5VejgBjBk/v-deo.html