This video will walk you through various ways to establish MACO Value during cleaning validation, how to define swab limit and how one can identify worst case scenario
Пікірлер: 48
@anuragprakashtiwari18392 ай бұрын
Nyce
@prasangitv3658 Жыл бұрын
From long back am searching for this , now I got information about this , thank you professor
@subratmishra646811 ай бұрын
I want to give 1000000 likes for this Crystal clear clarity sir....
@amitgupta-yr5pl2 жыл бұрын
This is great presentation on cleaning validation
@Pharma-73589 ай бұрын
Iam Working in Cleaning Validation Department And it is So Useful
@dhirenheisnam9992 Жыл бұрын
Bless you, sir. It is so helpful .
@akashgondaliya85372 жыл бұрын
Excellent sir, superb explanation......
@yogeshpatel8860 Жыл бұрын
Very nice way to explain in detail,thank you sir
@anurai31782 жыл бұрын
Thank you for your video.. really helpful
@sivaprasadsiriki12412 жыл бұрын
Very interesting and can easily understood, thanks for valuble information thank you sir🙏
@dattashinde51012 жыл бұрын
Very nice sir easily understood how to calculate MACO value
@jonnadulapavan55482 жыл бұрын
Very informative session...Tq so much sir..
@buddepumohanarao83093 жыл бұрын
Very nice information and thank you sir
@pharmagrowthhub30833 жыл бұрын
Most welcome
@harikrishna8513 жыл бұрын
Thank you
@nareshbabuMekala2 жыл бұрын
Very helpful
@utkarshvyas31852 жыл бұрын
Thank you sir ...
@Learnwithsimon272 жыл бұрын
very nice explanation, sir.
@Swara4303 жыл бұрын
Very informative, thanks for sharing this 😊
@pharmagrowthhub30833 жыл бұрын
My pleasure 😊
@prasadmallavarapu77402 жыл бұрын
Thank you sir..........
@AmanYadav-tc4um2 жыл бұрын
Thank you sir 🙏
@mansouralajeemi91012 жыл бұрын
@vadlavallikanakarao3154 Жыл бұрын
Good information sir
@kiranpillalamarri45172 жыл бұрын
Superb bro
@tanajikadam24552 жыл бұрын
Very good
@rohitbrahmbhatt5462 Жыл бұрын
Sir me and my boss both are fan of you ... U r doing excellent job... Only one poin need to be consider that give reference of guidelines which make complete preparations of interview.😊😊😊
@bhavins2093 жыл бұрын
Sir, we are from pharma industry and your video has been really helpful in understanding the concept of cleaning validation. Can u please provide the reference documents or guidelines relevant to the data mentioned in this video as we are facing many queries on this topic during audits!
@dipakdeore2954 Жыл бұрын
Nice
@praveenmanapragada16842 жыл бұрын
Dear sir , Thank you for giving the valuable information . Here in conversion of µg/dm2 to ppm for swab , swab diluent volume taken as 10 ml .kindly explain how can i fix the volume of swab diluent.
@nehamansoor91446 ай бұрын
Is 1500 dm2 total surface area of equipment?
@babu2008103 жыл бұрын
Good presentation. How would the worst case scenario be determined when you have to consider solubility, colour, fragrance, PDE.
@pharmagrowthhub30833 жыл бұрын
God point. White in colour + highly insoluble in water = worst case
@gudiyakumari67743 жыл бұрын
@@pharmagrowthhub3083 ooooo
@HamzaElMouaffek6 ай бұрын
I have the same question, first you need to determine the worst case product by considering cleanability colors solubility... Then you have to calculate the worst case maco. Please feedback, if you find an answer.
@subhanid66562 жыл бұрын
Dear sir, please help me in how to development dissolution method for NMC molecule
@gulammuhiuddin8894 ай бұрын
How to calculate Maco of different product manufacture in same vessel by rinse method
@maheshupadhya73042 жыл бұрын
Fantastic interpretation Sir thank you.. Have a doubt on safety factor, for ex.how much to consider if the range of 10 to 1000 in case of topical, is it any number between 10 to 1000 suppose I select as 200 as safety factor or the maximum as 1000 how it is taken. Thankyou
@rohitbrahmbhatt5462 Жыл бұрын
10 should be take to get wort case of MACO value
@toplistsmania2845Ай бұрын
Plz answer 1.What is safety limit for injectable. How we calculate safety factor for specific API. 2. What will be the batch size. Is it total bach size of product or only quantity of API in batch.
@mmh78172 жыл бұрын
Sir how to set the limit for that product whose MACO is less than LOQ AND LOD which guidelines to be followed kindly suggest.
@prafuldineshgawadgawad346111 ай бұрын
Hiii sir how to define acceptance limit in ppm for cleaning validation
@heisenberg_chemАй бұрын
Can i get pdf for reference
@rohitbrahmbhatt5462 Жыл бұрын
Sir how to calculate safety factor???
@sunilshedage95032 жыл бұрын
sir, how did you calculate MBS 5 Kg = 50 000 000 mg
@subhanid66562 жыл бұрын
Bro 1kg=1000g 5kg=5000g So 1g=1000mg 5000g = 5000*1000mg=5000000mg I hope you understood
@faezabutt75802 жыл бұрын
Is there any training on cleaning validation by napte bhaskar? If anyone knows kindly share link please
@pharmagrowthhub30832 жыл бұрын
Live workshop on Cleaning validation: us02web.zoom.us/webinar/register/8416507954921/WN_b_S4Wk6rS-ukrLy8CBV9mQ