Is this cleaning validation shall be done with respect to every product on every equipment?? suppose in a non dedicated commercial manufacturing plant product A manufactured 10 batches on a row and for first three bathes company has performed cleaning validation, established dirty equipment hold time and cleaned equipment hold time as well, after product change over product B is going to manufacture in same equipment train which are used earlier for product A, now product A cleaning procedure, dirty hold time and cleaned equipment hold time is applicable for product B or not, please clarify.
Dear Gaurav, I will really like to take training on this topic, if approximate 10-15 participants are available. Request you to check with your subordinates and friends. Please confirm.
I suggest, you can go through complete cleaning validation package. You will get information on all sort of dosage forms.If you have any questions, please feel free to comment. Will revert you. You can access the cleaning validation package through the link below; ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-zA5xsWR9IU8.html
Sir i have a query for one cleaning validation. If my product concentration is 50 MCG per ml And batch size is 275 litre. What should is acceptance criteria.
We can not just evaluate by referring this information. I suggest, you refer our cleaning validation part- II for better understanding. I am sharing link for the same. ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-zBLqRZ5DXV4.html
The responsibilities are inprocess at shop floor, evaluate critical process parameters, evaluate cleaning activities and give line clearance before going ahead for new product so as to protect the next product from contamination. Now a days, IPQA role is considered as Quality facilitator.
very informative. I subscribed to your channel and watched most of your videos. Subtitle is always useful. Thanks for adding it. Now I can follow and understand your explanations.
Thanks and welcome. Keep Learning !!! The video will be available soon on,"Inspection Readiness for computerised systems". You will get notification shortly about it if, you have activated notification icon(BELL) button.
For cleaning validation after vaccine product, we need to evaluate what factors will impact on next products e.g. antigens of previos virus vaccines, the chemicals used for attenuation etc. We need to evaluate traces of these antigens or chemicals. It all depends on process followed. If you specify in detail, can guide you in better way.
This training video will insight on Cleaning Validation - Inspection observations, Visual clean criteria & Solving practical problems during cleaning validation.
