Equipment Validation I Pharmaceutical Industry l DQ IQ IQ PQ

[@5669262309]

Thank you madam. And ur explanation is very simply understand anyone. Thank you. Plz send that link about remaining validations.

[@simplifypharma]

I will upload those videos asap

[@simplifypharma]

Kindly refer the channel for more validation videos

[@TheNyakaat]

Very clear explanation!

[@PHARMAACQUAINTANCE]

Wow very helping video 😊😊😊

[@ashishgajjar7056]

Very useful video, easy to learn method with easy examples. Nice ma'am 🎉

[@abdullahalasri6682]

Thank you for the effort and clear well explained presentation

[@simplifypharma]

Your comments are what keep me motivated

[@RAJATSAYYED]

Very nicely explained

[@playlistajsy4486]

Will you please elaborate each phase of equipment qualification with listed (1) how design protocol, what is the basic approach and require thing to design protocol, reference of protocol design (2) any common considerations in protocol design irrespective of equipment make mechanism function etc. Eg. Safety, risk assessment, challenge studies, product runs like that are any more. (3) what we have to do if we observed non intrensic failures of equipment qualification (4) how to schedule calibration, preventive maintenance (5) how we can recommend preventive maintenance, in what way, what we need, and references of preventive maintenance etc etc

[@simplifypharma]

I will try and upload the videos

[@carlasims6461]

Mnnnn I’m in love

[@carlasims6461]

I

[@carlasims6461]

Lovrs

[@ashishgajjar7056]

Yes ma'am, please provide video regarding protocol​@@simplifypharma

[@argentosebastian]

What gmp stand for?

[@simplifypharma]

Good Manufacturing Practices