21 CFR Part 11 | Electronic Records & Electronic Signatures | GxP Computer System requirements

The presentation discusses details of 21 CFR Part 11 requirements and guidance for industry for the same.
Details of Part 11 requirements for Electronic Records, Electronic Signatures, Validation of Computerized System, Audit trail, Handwritten signatures has been explained.
Discretion of legacy system along with requirements for validation, retention has been defined.
About the channel:
The channel has been developed with view of sharing information on Pharmaceutical Guidelines & Guidance.
Kindly subscribe to channel at: / @proftalks1680

[@thetenderloins6564]

Thanks a ton for clearly explaining! Really helpful and crisp!

[@mohankumar914]

Clearly explained each section, thank you

[@proftalks1680]

Thank you very much

[@sumanthm1025]

Well explained Sir, looking forward for more videos from this channel

[@proftalks1680]

Thank you very much.. Working on the same

[@jemslee211]

Well elaborated sir👏
From
Kaushik Gupta

[@proftalks1680]

Thanks🙏

[@mohdzohair8702]

Nicely presented 👍

[@proftalks1680]

Thank you

[@7prageshsingh431]

Thanks sir

[@proftalks1680]

Thank you

[@dorrinasefi9400]

Thank you this is good do you have method to validate e signature software too

[@proftalks1680]

Thanks.. Will revert back

[@rakeshscetic]

very useful information. May I have your contract details..