Ultimate video on change management system I. e. From initiation to closure... Highly useful for all pharmaceutical employees especially who are involve in day to day change initiative and review.....
This is very important topic and now days regulators are more focusing on change control and it's impact on GMP environment.well explained in this video. Thanks for sharing you knowledge Bank for us.
Congratulations Sunil! Wonderful initiative to give back to the Pharmaceutical Industry, which has given us so much. Appreciate your willingness to train Pharma professionals who can learn cGMP when they have time. As conveyed I will ask our QA managers to use these Videos as Training program for one and all with some snacks, which you will miss. Bravo to you! This will be your best wealth. Keep it up.
This is very informative video. Specially, level 1, 2 and 3 classification and based on severity assessment/ required documentation of change control. This video is very important for every pharma person responsible directly or indirectly for change control. managment.. Eagerly waiting for next video.... 3
Sir , Thanks for sharing. This is very informative video. Specially, level 1, 2 and 3 classification and based on severity assessment/ required documentation of change control. This video is very important for every pharma person responsible directly or indirectly for change control. managment.. Eagerly waiting for next video....
Thank you so much for sharing your experience on this plateform. Sir please make a vedio on risk assessment. Your way of explaination is very nice. Good luck and waiting for your next vedio. Thanks
Change control example with full format each n every steps covered, all documents that we need to attach... What barrier comes to deal with qa, production,hods, qc to reach approval, closure, kindly upload the video
if ccf is initiated to perform protocol base activities for data generation purposes. what is category for this ccf. Effectiveness is required for this ccf?
Elaboration of analytical procedure will be consider under what level??? For example--- We are fixing grade of chemicals in STP based on experience and validation. Elaborate Standard and sample preparation ---- what care to be taken for handling standard and sample. Elaboration of sample preparation---- how to shake the flask.
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Ultimate video on change management system I. e. From initiation to closure... Highly useful for all pharmaceutical employees especially who are involve in day to day change initiative and review.....
Yes.
This is very important topic and now days regulators are more focusing on change control and it's impact on GMP environment.well explained in this video. Thanks for sharing you knowledge Bank for us.
Excellent presentation in detailed
Glad you liked it!
Very useful to all Pharma professionals
Must needed to learn as per current expectations of all regulatory
Congratulations Sunil! Wonderful initiative to give back to the Pharmaceutical Industry, which has given us so much. Appreciate your willingness to train Pharma professionals who can learn cGMP when they have time. As conveyed I will ask our QA managers to use these Videos as Training program for one and all with some snacks, which you will miss. Bravo to you! This will be your best wealth. Keep it up.
Thank you so much sir for your appreciation and recognising the value of videos which is the need for every freshers in pharma professional.
Your video is exactly...good
I seen all video ...
Thanks and welcome
This is very informative video. Specially, level 1, 2 and 3 classification and based on severity assessment/ required documentation of change control.
This video is very important for every pharma person responsible directly or indirectly for change control. managment..
Eagerly waiting for next video....
3
Thank you.
Sir , Thanks for sharing.
This is very informative video. Specially, level 1, 2 and 3 classification and based on severity assessment/ required documentation of change control.
This video is very important for every pharma person responsible directly or indirectly for change control. managment..
Eagerly waiting for next video....
Sure!
nice presentation
Good information.....need to make video regrading new product introduction through CC. with case study.
Sure I will
Very useful Video. Thank you sir.
Thank you.
Thank you so much for sharing your experience on this plateform.
Sir please make a vedio on risk assessment.
Your way of explaination is very nice. Good luck and waiting for your next vedio.
Thanks
Sure.
Thank you.
Nice sir, & thanks for giving valuable knowledge.
Tq sir valuable information please provide 21CFR and CAPA related videos also sir
Ok sure
Well explained 👍👍
Change control example with full format each n every steps covered, all documents that we need to attach... What barrier comes to deal with qa, production,hods, qc to reach approval, closure, kindly upload the video
Very well explained thank you so much. Could you please make the procedure for deviation management as well.
Yes, soon
TQ sir
Thank you sir for sharing
So nice of you
Thankyou sir...
Good evening sir
Please give clarity between temporary change control and plane deviation.
Both are almost same, just difference in presentation. As per guideline, there is only deviation.
Sir !
TCC now undergo deviation is it correct !
if ccf is initiated to perform protocol base activities for data generation purposes. what is category for this ccf. Effectiveness is required for this ccf?
nice
Sure.
Thank you.
How manual tracking to be done for change control
Tracking will be difficult once number will increase. We should have software based control.
Provide risk assessment procedure for proposed changes
Sure.
How to write the change control log book for periodic review
Elaboration of analytical procedure will be consider under what level???
For example---
We are fixing grade of chemicals in STP based on experience and validation.
Elaborate Standard and sample preparation ---- what care to be taken for handling standard and sample.
Elaboration of sample preparation---- how to shake the flask.
It depends, based on factors and parameters which has impact on analytical results shall be elaborated. I agree with examples you have mentioned.
@@SunilSingh-wg9sh I assume it will be level 1 change...... right!!!
thank u sir
How to identify the design of compression machine? Which impact on regulatory filling.
First of all, note down all your requirements then search the machine which can meet your requirements.
How to closer change control in detail
Hello Sir I think u were in Ranbaxy
Yes
WHAT ABOUT CROSS FUNCTIONAL TEAMS SIR
Hai sir goodmorning plz explain with examples with documents (case studies different type) plz share me
Sir please share method verification
Hello sir