3 stages and 4 types of Process Validation | FDA Guidance on process validation

[@rajeshpaskanti8345]

Good👍

[@vaidikchetanmanch4858]

Super se bhi upar

[@PrasannaKumar-vm9rt]

Can you describe simply by denoting giidline name and number along with 21 cfr, anvisa , ich, other guidelines. Means Which guidelines refer to validation, qualification, investigation, risk assessment, change control, deviation, incidents, capa, root cause analysis, sampling techniques, manufacturing and packing, gdp, gmp. Etc Plz awaited for response.

[@sailalith1989]

Excellent it's helpful for me am IPQA Chemist.

[@arvindrajput986]

Bro....Where? City

[@rutujapatankar19]

Nicely explained. Thankyou

[@pharma8975]

Nice explanation and superb

[@IK-qu9hw]

Very nice. I am instrumentation engineer 2017 batch. After completion of degree I started working in automation field ( I have done oq ,pq of blender, RMG ,FBD machine also 21 cfr part 11 with end client. ) now I have 1 yr experience in automation field.since salary package is very less so now I am thinking to switch to pharma sector, I have one question what should I do now shall I switch to pharma or not? Plz reply..

[@vanjinathan6561]

Chicken TBH 4th CCTVbut v chubby

[@amitkumarshukla3234]

Very good explanation

[@Smittaji]

Audio is having too much base & subtitle is typing something which cannot be related to the conversation. good video, very hard to understand with the audio issues

[@badithalakishorekumar112]

Good information

[@ramuboppani9254]

Thanks for sharing

[@ParthPatel-wn6sp]

Please explain latest Process Validation theory.

[@pratikshawavale]

Thanks for the guidance .keep making more videos for pharma learner like me.

[@Indianvlogs143A1]

Tq excellent information

[@boinikrishna3364]

Sir in pharma IPQA vs AR&D which is best sir for better growth.. Please give me reply sir..

[@vinayak8055]

If long time years validation not done then there is need of revalidation ? Even there is no any change in process.OR It's available of any period of revalidation?

[@syedmuzamilshah8316]

superb

[@krishnanvisva4137]

Super sir

[@jigishapatel4487]

Sir, can you please explain Process validation for EMA also ?? How does it differ there ??

[@girijarithi6806]

Super

[@anilreddy1650]

Sir which guide line is supporting.

[@ajayspecial3936]

Superb

[@pharmalearners3120]

Thank you Ajay

[@niharranjanmeher4989]

Sir..Plz remove the background music...

[@kartheekgoud5385]

Sir, why 3 batches are required for process validation??

[@himanthmanne8447]

look at the FDA regulations

[@vishal11ism]

Two batches are not enough to provide statistic data, and 4 batches can be done but will be time consuming and pricey.

[@PharmaPill]

👍🏻

[@govardhanreddy1891]

How many batches to take for re- validation

[@ravinpawar8638]

Good ppt

[@munduruganesh3651]

👌

[@pharmalearners3120]

Thank you

[@khushbookanojiya749]

Gud video but Plz Hindi m bhi discribe kare

[@abhishekdhiman8222]

Sir... Background music ko band kare

[@Rakeshkumar-xo2xv]

Plz speak in Hindi......

[@pharmalearners3120]

Thank you Rakesh for your suggestion, I will definitely implement it in future

[@vijayaramakrishnapilli8583]

very nice explanation