Good Documentation Practices in Pharma Industries in Hindi & English

This video is about Good Documentation Practices in Pharma Industries in Hindi & English
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Good documentation practices
As per WHO TRS 996 Annex -5.Good documentation practices are those measures that
collectively and individually ensure documentation, whether paper or electronic
data is secure, attributable, legible, traceable, permanent, contemporaneously
recorded, original and accurate. Personnel should follow GDocP for both paper records and
electronic records in order to assure data integrity. These principles require
that documentation has the characteristics of being attributable, legible,
contemporaneously recorded, original and accurate (sometimes referred to as
ALCOA). These essential characteristics apply equally for both paper and
electronic records.
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Hello, Friends welcome to my channel "PharmaGyan" Learn about Pharmacy, Pharmaceutical companies, regulatory guidelines, Documentation procedures, SOPs, How to videos on various operating procedures, Quality Assurance, Quality control, R&D, Pharmaceutical validation and qualification guidelines and procedures etc.

[@abhinandanjain2399]

Thank you so much sir ji for this valuable video.

[@PharmaGyan]

Thank you

[@sajneeshrestha8168]

such a helpful video. Thank you!

[@ashokgunawat1104]

Awesome helpfull video.thank you

[@arvindgour9481]

Helpful video 🙏

[@domendrasahu4058]

Sir should have basic computer knowledge while doing B.Pharma which will be useful in future like industry

[@PharmaGyan]

Computer proficiency is must requirement in each and every field of pharma

[@vikaspachisia8248]

Nice 👍

[@shivrajwadekar9807]

Thnx

[@shubhammishra3753]

Method of teaching is very good, nice content

[@PharmaGyan]

Thanks

[@kalpeshnerkar4062]

Sir, in Pharma documentation main careers and salry growth acchi hai kya

[@Pharmaacenter]

Sir, can u please guide me that what is the skills required to be a good in regulatory affairs field?

[@PharmaGyan]

You need to know about basic regulatory requirements, for that you must read various regulatory guidelines, you must have knowledge of documentation procedures and documentation requirements of regulatory bodies, submissions and fillings to regulatory bodies.