Good Documentation Practices in Pharma Industries in Hindi & English
Вставка
- Опубліковано 4 жов 2024
- This video is about Good Documentation Practices in Pharma Industries in Hindi & English
Visit our website for more stuffs like guidelines, jobs, vacancies, SOPs, Protocols, etc.
Link is : sites.google.c...
Let's Checkout Our Other Videos
Good Documentation Practices in Pharma Industries- • Good Documentation Pra...
What are Regulations / Directives and Guidelines for Pharmaceutical Companies - • What are Regulations /...
21 CFR Part 11, Interview Questions and Answers | Electronic Records & Signatures | PART 1 of 2 - • 21 CFR Part 11, Interv...
Deviation Flow Chart | Unplanned Deviation Flow Chart : • Deviation Flow Chart |...
Deviation Part 2 of 2 - • Deviation in Pharmaceu...
Deviation Part 1 of 2 - • Deviation in Pharmaceu...
Qualification of Vial washing machine part 04 of 04, Visible Particle Removal Test : • Qualification of Vial ...
Qualification of Vial washing machine part 03 of 04, Residual Water Determination Test - • Qualification of Vial ...
URS in pharmaceutical companies : • URS in pharmaceutical ...
Change Control Flow Chart : • Change Control Flow Ch...
Top 10 pharmaceutical companies in world in case of revenue : • Top 10 Pharmaceutical ...
Qualification of Vial washing machine part 02 of 04, insoluble matter removal study : • Qualification of Vial ...
Qualification of Vial washing machine part 01 of 04: • Qualification of Vial ...
List of ISO Guidelines : • ISO Guidelines List
Clean room classification by ISO : • Clean Room Classificat...
Validation of Autoclave and Qualification Part 1: • Validation of Autoclav...
WFI Specifications : • WFI Specifications for...
Steam Sterilization or Autoclaving Basic concepts Part 02 of 02: • Steam Sterilization or...
Pharma technical series interview questions and answers : • Pharma Technical Serie...
Incident - • Incident in Pharmaceut...
Types of Thermocouples - • Types of thermocouples...
GMP History - • GMP History| How GMP C...
GMP Vs cGMP - • GMP VS CGMP | Differen...
Types of Validation - • Validation in hindi | ...
Trick to remember 21 CFR - • Trick to remember 21 C...
Concept of ALCOA or Data integrity - • Data integrity in Phar...
Concept of ALCOA or Data integrity - • Data Integrity in Phar...
APQR - • APQR | Annual Product ...
CAPA - • CAPA | Corrective Acti...
Tablet manufacturing process - • Tablet manufacturing p...
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.
#PharmaGyan
#GDocP
#GDP
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.
such a helpful video. Thank you!
Awesome helpfull video.thank you
Thank you so much sir ji for this valuable video.
Thank you
Sir should have basic computer knowledge while doing B.Pharma which will be useful in future like industry
Computer proficiency is must requirement in each and every field of pharma
Helpful video 🙏
Sir, in Pharma documentation main careers and salry growth acchi hai kya
Method of teaching is very good, nice content
Thanks
Nice 👍
Sir, can u please guide me that what is the skills required to be a good in regulatory affairs field?
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.
Thnx