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Tq sir 😊

Thank you sir clearly explained

Exlent explain sir

Thank you so much sir

Correct ga explain chesaru, it is real process in api Pharma plant

Sir risk assement cheppandi sir

Sir update ayina guideline prakaram oka video cheyyandi sir

Crystal clear explanation sir

Nice sir tq🙏

Nu super anna

Nice explanation sir

thank you brodar

Very useful information

Sir, Please do the vedieo clean room procedure.

Method -I in MBS -minimum batch size (next ), you're told maximum batch size noted sir

Very nice sir 👌

Not satisfy update your skills

Thank you sir i got more knowledge from your vedio

Q

Kindly prepare in Hindi

Super sir more vedies cheyandi

Me explanation chala bagundhi sir

Nice sir

Excellent sir

Great sir

Good explanations

It s useful to all pharma employees who is working in big and small companies

Thank you sir from maharashtra requesting you for english exeplenation

Sir please give a class for Process capability,Cpk ,Cp & Continued process verification.

Do you have any notes regarding csv

Hello sir....why share slide show...peoples want to how to fill form and investigation with any examples....

Sir,Can you please explain about APQR and how to do process capability

TQ

Sir chlorination grignard reaction

nice sir

thanq sir for clear info. about process validation

Super sir .... excellent....sir...class...

Thank you sir

Sir how to face auditor video and auditor questions tell me

Thanks sir

Thankyou sir

sir how can I consider the previous product or the next product in MACo calculation please reply 🙏

Dear sir, Introduction of new product through change control?

TQ sir

Low voice level

Valuable information

Plse suggest guide line name for Process and cleaning validations..

Very nice explanation sir

1qqq

THANX DOCTOR PLEASE IN FUTURE IF YOU CAN DO VIDEO BY ENGLISH LANGUAGE I WATCHING YOUR VIDEOS FROM LIBYA