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.
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.....
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.
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....
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 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.
