GVR Pharma tutorial

17:37

What is Equipment Qualification, Stages of Qualification

2 ай бұрын

1:21

What is 5s in pharmaceutical industry,What are the benefits of 5S.

2 ай бұрын

1:14

What is FIFO(first-in,First-out),What is FEFO (First-Expired,first-out)

2 ай бұрын

1:16

Job's in Visakhapatnam (Vizage) for Freshers only

4 ай бұрын

1:26

Pharma Jobs In Vizage & Hyderabad, Interview location: Vizage, Year of passing: 2023 & 2024

5 ай бұрын

1:32

Jobs for M.Sc Chemistry Candidates, Year of Passing : 2023 & 2024

5 ай бұрын

6:48

What is Retrospective Validation ?,

5 ай бұрын

1:10

location: Visakhapatnam, Jobs in Dr.Reddy's labs for freshers #job #jobsearch #pharma

5 ай бұрын

20:12

What is Validation?, Why do we Use 3 Batches for Validations

5 ай бұрын

1:15

Pharma job's for B.Sc /M.Sc /B.Tech Freshers Only

5 ай бұрын

1:22

Pharma job's In VIZAGE & Hyderabad for Male & Female candidates, Interview Location: VIZAGE

5 ай бұрын

1:32

jobs for freshers in DR.Reddy's srikakulam,

6 ай бұрын

1:09

Job's for Women's only, Jobs in Reliance Life Sciences

6 ай бұрын

1:10

Pharma Jobs for freshers, Qualification:B.Sc, B.Com,B.A

6 ай бұрын

14:47

What is Concurrent Validation, When to Perform Concurrent Validation.

6 ай бұрын

11:25

What is Prospective Validation ? , When to Perform Prospective Validation

6 ай бұрын

2:08

Stages of process validation(Process Design,Process Qualification, Continuous process Verification )

7 ай бұрын

10:23

Process validation,Types of process validation,prospective,Concurrent,Retrospective validation

7 ай бұрын

10:47

What is Validation? , Importance of Validation !, Types of Validations ?

7 ай бұрын

1:07

Jobs for Experience Candidates,Department: Production,Experience: 2-5 years,Location: Visakhapatnam

8 ай бұрын

1:12

Pharma job's for M.Sc /B.Sc(Biotechnology / Biochemistry/Microbiology/Genetics),B.Tech-Life science

8 ай бұрын

1:18

Pharma job's for freshers & Experience Candidates Qualification: 10th, Intermediate ,Any degree

8 ай бұрын

2:03

Jobs for Experience Candidates in MSN Labs, Experience:1-8 Years, Departments: Production & ESD

8 ай бұрын

13:03

What is GMP ?(Good manufacturing practice), What is cGMP ?(Current Good manufacturing practice)

8 ай бұрын

0:58

Pharma interview questions for Experience Candidates

10 ай бұрын

1:06

Jobs for B Pharmacy & BSc(Chemistry) freshers in HETERO Labs

10 ай бұрын

1:04

jobs for Experience Candidates,Experience:3-9 Years, Qualification:B Tech/Diploma/ITI Fitter

10 ай бұрын

1:07

Jobs for Experience Candidates, Department: Production & Documentation,QC, Engineering, Warehouse.

10 ай бұрын

1:07

Jobs for Experience Candidates, Department: Production & Documentation,QC, Engineering, Warehouse.

10 ай бұрын

Пікірлер

@SonuSingh-bx9gc Күн бұрын

Brother please give me ur Number urgent

@Viratram464 2 күн бұрын

Nice

@SonuSingh-bx9gc 3 күн бұрын

Please respond

@SonuSingh-bx9gc 3 күн бұрын

Hi brother vacuum distillation pttinapud temperature enduk down autundi

@PavanshannuTammina 3 күн бұрын

Sir can you explain about conductivity principle and how it works

@Paddupapaaaaa 3 күн бұрын

Sir polarography gurinchi cheppandi sir plssssss

@MatamGurunathswamy 7 күн бұрын

Oil name?

@MatamGurunathswamy 7 күн бұрын

+5 lo ememi vuntai

@SANDEEPKUMAR-gk9mm 7 күн бұрын

Electronic configuration All salvents explain sir please

@isovenu 11 күн бұрын

Good presentation 👍

@AUupdates2024 16 күн бұрын

Sir, How to validate a new plant It means handover from wender to Clint This is rapid kids manufacturing unit Please make a video sir

@ravi-GR 16 күн бұрын

Hvd system gurinchi, Fraction distillation gurinchi video cheyandi brother.. Plsss

@ravi-GR 21 күн бұрын

Tq so much brother 👌👌, HVD reactors and process gurinchi kuda video cheyyandi brother.

@ramaiahramu9392 22 күн бұрын

Vacuum pump types video cheyandi sir

@ramaiahramu9392 22 күн бұрын

Great job sir

@Srinu_from_vizag 22 күн бұрын

Very class sur

@pavankalyan7266 23 күн бұрын

ANFD కి కాండెన్సర్(H.E )ఉండదా..???

@kamesshrao5493 24 күн бұрын

Nice explanation sir thankyou

@ramaiahramu9392 25 күн бұрын

Sir please explain atfd equipment

@telugulyricsram 26 күн бұрын

Nice explanation sir 👏

@thiruveedulasrikanth25 28 күн бұрын

howmuch dp we have to maintain to room to room sir in 3 types of airlock?

@lavanyakyatham-1968 29 күн бұрын

Hphv and vph auto sterilization video provide sir

@user-xo5ny2js9t 29 күн бұрын

O.2 micron hydrofolic filters tho filtration avadam ledu reaction mass kuda water Loni vundi enduku avadam ledu sir

@MohanRoyalcreations 29 күн бұрын

Reflex line ki బెండ్ ఎందుకు పెడతారు చెప్పండి

@amourya3159 29 күн бұрын

Sir first thing meeru okati telusukovali mi channel ni chustunnarantene ardham vallu pharma industry ki relatedt ani video 20min ithe 14min above waste cheppinattu anipinchindi naku

@amourya3159 29 күн бұрын

Sir HEPA Filter gurinchi chepparu kani danni ela cheyali anedi cheppaledu

@saikumarganta9281 Ай бұрын

Sir, Reactor,ANFD EOR ల గురించి కూడా ఎక్సప్లెయిన్ చేయరా sir...

@saikumarganta9281 Ай бұрын

Thank you soo much sir...

@naturalfarm8404 Ай бұрын

Anfd rpm antha vuntundi

@kotikakaraparthi8080 Ай бұрын

Power pothe..... agitator kuda ayipothundiiiiiii ga, because motor agutundi ga

@AnithaBagathi Ай бұрын

Sir females ki leda

@gnaneshwarondra9026 Ай бұрын

Very nice Teaching sir thank you so much

@gandamanuchinnarao5028 Ай бұрын

Centrifugal lu inches lo vuntaya

@srinivasb7005 Ай бұрын

Sir please post about hydrogen reactions that it will be very useful to us

@ramireddyramagangireddy7146 Ай бұрын

Crystalyztion factors effecting video cheyandi sir your videos very good.

@princehymad3664 18 күн бұрын

CGmp gurinchi chepandi

@skassan8000 Ай бұрын

Super explanation sir

@satishkumar-yp1sv Ай бұрын

Traceable which guidance is recommended Please give the link of link

@gvrpharmatutorial Ай бұрын

ALCOA++: Further Enhanced Focus ALCOA++ incorporates modern requirements and technological advancements: 1. Integrity: Systems should ensure data is protected from unauthorized modifications or loss. 2. Timeliness: Data management processes should ensure swift and appropriate recording of information. 3. Reproducibility: The system should enable verification and reproduction of results or operations.

@gvrpharmatutorial Ай бұрын

Global Guidelines Supporting ALCOA FDA: 21 CFR Part 11 outlines requirements for electronic records and signatures. WHO: Guidelines on Good Data and Record Management Practices. EMA: Guidelines for ensuring data integrity in the pharmaceutical quality system.