- Видео 48
- Просмотров 518 010
EASY QUALITY LEARNING
Индия
Добавлен 3 мар 2020
EASY QUALITY LEARNING ABOUT SHARING THE LEARNING AND EXPERIENCE ABOUT PHARMACEUTICAL QUALITY TOPICS. THIS WILL INCLUDE THE SUBJECT'S AND TOPICS WHICH WE WILL COME ACROSS IN EXECUTION OF OUR ROUTINE QUALITY CONTROL AND QUALITY ASSURANCE ACTIVITIES.
ANALYTICAL BALANCE CALIBRATION IN HINDI
THIS VIDEO IS USEFUL FOR THE PROFESSIONALS OF QA, QC, AD. THIS VIDEO WILL GIVE INSIGHT ABOUT THE ANALYTICAL BALANCE CALIBRATION AND ITS QUALIFICATION. THIS VIDEO WILL ALSO GIVE THE INFORMATION THAT HOW MINIMUM WEIGHING CAPACITY OF THE ANALYTICAL BALANCE IS DETERMINED.
Просмотров: 294
Видео
ALCOA PLUS IN ENGLISH
Просмотров 3542 месяца назад
ALCOA PLUS IS USEFUL VIDEO FOR ALL THE PROFESSIONALS AND NEW LEARNERS OF QA, QC, PRODUCTION, ENGINEERING, IT, R&D. IT WILL GIVE THE INSIGHT ABOUT THE DOCUMENTION PRACTICES ON PAPER BASED AS WELL AS COMPUTER SYSTEM. EACH PARAMETER IS EXPLAINED WITH VERY EASY EXAMPLES.
GOOD LIQUID CHROMATOGRAPHIC PRACTICES IN HINDI
Просмотров 4553 месяца назад
THIS VIDEO WILL DESCRIBE ABOUT THE STANDARD PRACTICES TO BE FOLLWED IN LIQUID CHROMATOGRAPHY IN EASY LANGUAGE. IT WILL ALSO EXPLAIN ABOUT THE PRECAUTIONS TO BE TAKEN DURING MOBILE PHASE PREPARATION, COLUMN SELECTION, METHOD PREPARATION, BATCH TABLE PREPARATION AND ITS EXECUTION. IT WILL ALSO DESCRIBE ABOUT INTEGRATION, AUDIT TRAIL, BACKUP PROCEDURES AND OTHER RELATED ISSUES. THIS VIDEO IS USEFU...
DATA INTEGRITY IN HINDI
Просмотров 5494 месяца назад
THIS VIDEO WILL GIVE THE INFORMATION ABOUT THE DATA INTEGRITY PRACTICES AS PER WHO & PICS GUIDELINES. HERE THE PRACTICES TO BE FOLLOWED FOR DATA INTEGRITY FOR PAPER BASED SYSTEM AND COMPUTER BASED SYSTEM. THIS VIDEO IS USEFUL FOR ALL THE PROFESSIONALS OF QA,QC, PRODUCTION, ENGINEERING, R&D.
REVISED SCHEDULE-M MAIN PRINCIPLES (HINDI)
Просмотров 1,5 тыс.5 месяцев назад
THIS VIDEO WILL UPDATE ABOUT THE MAIN PRINCIPLES OF REVISED SCHEDULE M IN VERY EASY HINDI LANGUAGE. MAIN ASPECTS OF SCHEDULE M ARE EXPLAINED. THIS VIDEO IS USEFUL FOR ALL THE PROFESSIONAL OF PHAMACEUTICALS WORKING IN QA, QC, PRODUCTION, ENGINEERING, R&D, HR AND IT ALSO.
REVISED SCHEDULE M DIFFERENCES
Просмотров 3,2 тыс.6 месяцев назад
THIS VIDEO WILL GIVE THE INSIGHT ABOUT THE REVISED SCHEDULE-M AND WILL EXPLAIN ABOUT THE DIFFERENCES BETWEEN OLD SCHEDULE M AND REVISED SCHEDULE M IN VERY EASY LANGUAGE. THIS VIDEO WILL BE USEFUL TO ALL THE PROFESSIONALS RELATED TO PHARMACEUTICAL MANUFACTURING IN ANY WAY.
QUALITY RISK MANAGEMENT IN HINDI
Просмотров 2,7 тыс.Год назад
THIS VIDEO WILL WILL DESCRIBE ABOUT PROCEDURE OF QUALITY RISK MANAGEMENT IN PHARMACEUTICALS IN VERY EASY LANGUAGE. REFERENCE OF GUIDELINES AND EXAMPLES OF RISK MANAGEMNT ARE ALSO DISCUSSED. THIS VIDEO IS USEFUL FOR QA, QC, PRODUCTION, ENGINEERING AND R&D.
ALCOA PLUS IN HINDI
Просмотров 14 тыс.Год назад
THIS VIDEO IS USEFUL FOR QA, QC, R&D, PRODUCTION AND ENGINEERING DEPARTMENT. THIS VIDEO WILL DESCRIBE ABOUT EACH ELEMENTS OF ALCOA PLUS AND ALSO EXLAINED ABOUT EACH ELEMENT WITH EXAMPLE IN VERY EASY LANGUAGE. THIS WILL ALSO GIVE INSIDE ABOUT USAGE OF ALCOA PLUS PRINCIPLE IN PAPER BASED AS WELL AS COMPUTER SYSTEM.
VALIDATION OF STEAM STERILIZATION IN HINDI
Просмотров 606Год назад
THIS VIDEO IS USEFUL FOR THE PROFESSIONALS OF QA, QC, MICROBIOLOGY AND R&D. THIS VIDEO EXPLAINS THE PROCEDURE OF VALIDATION OF STEAM SFTERILIZATION IN VERY EASY LANGUAGE. REFERENCES OF GUIDELINES FOR STEAM SFTERILIZARTION IS ALSO MENNTIIONED FOR EASY UNDERSTANDING. THIS VIDEO WILL ALSO TELL ABOUT THE PRACTICAL ASPECTS OF STEAM STERILIZATION.
CROSS CONTAMINATION CONTROL IN HINDI
Просмотров 1,6 тыс.Год назад
THIS VIDEO IS USEFUL FOR QA, QC, R&D AND ENGINEERING PERSONNEL. THIS VIDEO WILL GIVE THE INFORMATION ABOUT THE CROSSCONTAMINATION AND ITS FACILITY LEVEL AS WELL AS PROCEDURAL CONTROL. THIS WILL EXPLAIN THE CROSS CONTAMINATION CONTROL IN A VERY EASY LANGUAGE.
GOOD MICROBIOLOGY PRACTICES IN HINDI
Просмотров 1,9 тыс.Год назад
THIS VIDEO GIVES THE INSIDE ABOUT THE MICROBIOLOGICAL PRACTICES WHICH NEED TO BE FOLLOWED IN MICROBIOLOGY LABORATORY. THIS VIDEO IS USEFUL FOR THE QC, QA AND R&D PERSONNEL. THIS VIDEO WILL BE ALSO USEFUL FOR MICROBIOLOGY STUDENTS.
PHARMACEUTICAL QUALITY SYSTEM IN HINDI
Просмотров 4,4 тыс.Год назад
THIS VIDEO WILL GIVE THE INSIGHT ABOUT PHARMACEUTICAL QUALITY SYSTEM AS PER ICH Q10 GUIDELINE IN VERY EASY LANGUAGE. THIS VIDEO IS USEFUL FOR ALL THE PROFESSIONALS OF QA, QC, R&D AND OTHER VERTICALS OF PHARMA AS WELL AS FOOD AND COSMETICS ALSO.
MEDIA FILL IN ENGLISH
Просмотров 1,8 тыс.2 года назад
THIS VIDEO EPLAINS THE MEDIA FILL ACTIVITY IN VERY EASU LANGUAGE, IT ALSO INCLUDES THE GUIDANCE INFORMATION, ELEMENTS OF ASEPTIC PROCESS SIMULATION AND PROCEDURE ALONG WITH LIMIT AND INTERPRTATION OF MEDIA FILL RESULTS. THIS VIDEO IS USEFUL FOR ALL MICROBIOLOGISTS, MANUFACTURING PERSONNEL, ENGINEERING PERSON AND R&D PROFESSIONALS.
MEDIA FILL STUDY IN HINDI
Просмотров 3,7 тыс.2 года назад
THIS VIDEO WILL DESCRIBE ABOUT THE MEDIA FILL ACTIVITY IN WHICH GUIDANCE DOCUMENTS, ELEMENTS OF MEDIA FILL, AND EXECUTION OF MEDIA FILL. THIS VIDEO IS USEFUL FOR PRODUCTION, QA, QC AND ENGINEERING PERSONNEL. ALL THE ACTIVITIES STEP WISE ARE EXPLAINED IN VERY EASY LANNGUAGE.
RESIDUAL SOLVENTS ICH Q3C IN HINDI
Просмотров 4 тыс.2 года назад
THIS VIDEO IS USEFUL FOR THE PHARMA PROFESSIONALS INVOLVED IN QA, QC, R&D, RA AND PRODUCTION ACTIVITIES. IT WILL BE EXPLAINED THAT WHY IT IS NECESSARY TO RESTRIC THE ORGANIC SOLVENTS IN THE PHARMACEUTICAL AND FOOD PRODUCTS. IT WILL ALSO DISCUSS THE CLASSIFICATIO N OF SOLVENTS AS PER ICH AND OTHER REGULATORY GUIDELINES AND HOW TO CONTROL AND EVALUATE IT.
SIGNIFICANT CHANGES IN STABILITY STUDIES HINDI
Просмотров 1,2 тыс.2 года назад
SIGNIFICANT CHANGES IN STABILITY STUDIES HINDI
OUT OF SPECIFICATION PART 2 IN HINDI
Просмотров 8 тыс.2 года назад
OUT OF SPECIFICATION PART 2 IN HINDI
OUT OF SPECIFICATION PART I IN HINDI
Просмотров 15 тыс.2 года назад
OUT OF SPECIFICATION PART I IN HINDI
ANALYTICAL METHOD VALIDATION OF IMPURITIES IN HINDI
Просмотров 14 тыс.3 года назад
ANALYTICAL METHOD VALIDATION OF IMPURITIES IN HINDI
DEVELOPMENT & VALIDATION OF CLEANING METHOD IN HINDI
Просмотров 4 тыс.3 года назад
DEVELOPMENT & VALIDATION OF CLEANING METHOD IN HINDI
PROCESS VALIDATION IN PHARMACEUTICALS
Просмотров 6 тыс.3 года назад
PROCESS VALIDATION IN PHARMACEUTICALS
Great presentation sir, always motivates and knowledgeable videos provided by you.🎉🎉
Very useful information.
Thanks
We should use analytical balance with least count of 0.1 mg or 0.01mg.
In pharma lab wcich balance we should use
Nice information
Nice information
Bahut badhiya tarike se samjhaya gya hai es vedio m
Very nice sir Thanks 🙏
This is gud information clean and clear simplae way
Sir apne bhut hi clearly describe Kiya h
Nice sir
Nice information
Very good video.. Lot's of learning.. Thanks
Very usefull
Sir, If the specification of API supplied by different vendor is same (no difference) then what to do
Nice video sir🎉
Sir, i think hardness test not at coated astage its only for core tab
Nice information sir
Very informative sir
Very nice sir
Very nice information
Sir complete guideline kaise download kare
Identified impurities0.2% hai to identified q nhi karte h .2143 hai
Nice information sir
Very nice explanation. Thanks a lot. very helpful and understood easily
Thank you sir
Thank you sir!
😊
Sir we need all ich guidelines in brief in hindi
Videos on ich Q1, Q2, Q3A, B, Q3C, Q6, Q9 & Q10 is already available on my channel, please refer to it.
Data integrity?
Data integrity is already uploaded on my channel
Data integrity?
ruclips.net/video/GzOzE-rXo80/видео.htmlsi=CJEdPw7I2rcjDwp9
Meaning of Alcoa application? Regards of data entry?
Please upload video
English version please
Already available on channel, please check
Nice 🤠 sir
Very useful and clearly explained point....
Thank you so much sir for simplification
Very good Sir ji
Very good information sir
Great sir ji..
Very useful Sir... Thanks 🙏🙏
Nice video
Very good video
Sir please explain detail calculation of TDI ?? How to calculate the value of TDI
It is total daily intake. Formula for TDI is Impurity result x maximum daily dose x 1000 / 100 Results will be in mcg if dose is in mg
Sir please explain detail calculation of TDI ?? How to calculate the value of TDI
nice
Sir you are making all video we are learning and very easy way understanding for me
Excellent presentation. It's a complete package about data integrity expectations in a simplest form. Thanks a lot Sir.
Best information sir