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Indian Laboratories Forum
India
Приєднався 19 лис 2021
We are launching free courses for laboratory professionals , manufacturing professionals, Formulation and Research and development professionals, and Student to grow in their careers by enhancing their knowledge. Follow us on UA-cam for updates on new courses.
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cGMP Subpart -D- Equipment - 21 CFR Part 211, ICH Q7, EU GMP
It details about the requirements of Equipment as per 21 CFR Part 211.
#QualityAssurance #Productconsistency #Documentation #Processvalidation #equipmentmaintenance #Calibration #QualityControl #personneltraining #Rawmaterialstandards #Manufacturingenvironment #Regulatorycompliance #Batchproductionrecords #Labelingcontrol #drugquality #stabilitytesting #cleanliness #sanitation #qualitycontrolunit #QCU #packaging #Labelingoperations #sampling #Testing #Changecontrol #Recordkeeping #Qualitsystem #Drugmanufacturing #Processingcontrols #Documentation&Records #Facilityrequirements #Equipmentmaintenance #Validation #Procedures #Personnelrequirements #Complainthandling #Recallprocedures #qualitymanagementsystem #Activepharmaceuticalingredient #API #ProductionandProcess Controls #Supplierqualification #Analyticalmethods #ValidationofAnalyticalProcedures #Stabilitytesting #Documentationpractices #Changecontrolprocedures #Training #Competence #regulatorycompliance #education #science #pharmacy #chemistry #biology #biotechnology #lifescience #biological #usfda #cdsco #fda #mhra #TGA #emea #nabl #iso9001 #9001 #iso17025 #laboratory #USFDAwarningletters #warningletters #FDA483 #educational #microbiology
#QualityAssurance #Productconsistency #Documentation #Processvalidation #equipmentmaintenance #Calibration #QualityControl #personneltraining #Rawmaterialstandards #Manufacturingenvironment #Regulatorycompliance #Batchproductionrecords #Labelingcontrol #drugquality #stabilitytesting #cleanliness #sanitation #qualitycontrolunit #QCU #packaging #Labelingoperations #sampling #Testing #Changecontrol #Recordkeeping #Qualitsystem #Drugmanufacturing #Processingcontrols #Documentation&Records #Facilityrequirements #Equipmentmaintenance #Validation #Procedures #Personnelrequirements #Complainthandling #Recallprocedures #qualitymanagementsystem #Activepharmaceuticalingredient #API #ProductionandProcess Controls #Supplierqualification #Analyticalmethods #ValidationofAnalyticalProcedures #Stabilitytesting #Documentationpractices #Changecontrolprocedures #Training #Competence #regulatorycompliance #education #science #pharmacy #chemistry #biology #biotechnology #lifescience #biological #usfda #cdsco #fda #mhra #TGA #emea #nabl #iso9001 #9001 #iso17025 #laboratory #USFDAwarningletters #warningletters #FDA483 #educational #microbiology
Переглядів: 125
Відео
Download Laboratories E learning portal app
Переглядів 1,2 тис.3 місяці тому
We are providing certificate courses for laboratory professionals , manufacturing professionals, formulation and research and development professionals, and students to grow in their careers by enhancing their knowledge. Download the app: play.google.com/store/apps/details?id=co.diy.undnw&pcampaignid=web_share #education #qualitycontrol #quality #regulatorycompliance #qualityassurance #english ...
Good Manufacturing Practices-Building Requirements 21 CFR Part 211, ICH Q7, EU GMP
Переглядів 1623 місяці тому
It details the requirements of buildings & facilities as per 21 CFR Part 211. #QualityAssurance #Productconsistency #Documentation #Processvalidation #equipmentmaintenance #Calibration #QualityControl #personneltraining #Rawmaterialstandards #Manufacturingenvironment #Regulatorycompliance #Batchproductionrecords #Labelingcontrol #drugquality #stabilitytesting #cleanliness #sanitation #qualityco...
Good Manufacturing Practices- Personnel Requirements 21 CFR Part 211, ICH Q7, EU GMP
Переглядів 1303 місяці тому
It details about the requirements of personnel as per 21 CFR Part 211. #QualityAssurance #Productconsistency #Documentation #Processvalidation #equipmentmaintenance #Calibration #QualityControl #personneltraining #Rawmaterialstandards #Manufacturingenvironment #Regulatorycompliance #Batchproductionrecords #Labelingcontrol #drugquality #stabilitytesting #cleanliness #sanitation #qualitycontrolun...
Good Manufacturing Practices, History, Introduction - 21 CFR Part 211, ICH Q7, EU GMP
Переглядів 6263 місяці тому
It will detail about the history of GMP, Purpose and Importance of GMP regulations in Pharmaceutical industries. #QualityAssurance #Productconsistency #Documentation #Processvalidation #equipmentmaintenance #Calibration #QualityControl #personneltraining #Rawmaterialstandards #Manufacturingenvironment #Regulatorycompliance #Batchproductionrecords #Labelingcontrol #drugquality #stabilitytesting ...
ISO/IEC 17025:2017, Clause 8.9 & Examples of NC's
Переглядів 5528 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 8.9- Management Reviews, and examples of nonconformances as per clause 8.9 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/boost/Jobs_Pharma_food_Industry keywords: ISO/IEC 17025, la...
ISO/IEC 17025:2017, Clause 8.8 & Examples of NC's
Переглядів 5118 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 8.8- Internal audits, and examples of nonconformances as per clause 8.8 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/boost/Jobs_Pharma_food_Industry keywords: ISO/IEC 17025, labor...
ISO/IEC 17025:2017, Clause 8.7 & Examples of NC's
Переглядів 4148 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 8.7 - Corrective actions, and examples of nonconformances as per clause 8.7 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/boost/Jobs_Pharma_food_Industry keywords: ISO/IEC 17025, l...
ISO/IEC 17025:2017, Clause 8.6 & Examples of NC's
Переглядів 3968 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 8.6 - Improvement, and examples of nonconformances as per clause 8.6 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/boost/Jobs_Pharma_food_Industry keywords: ISO/IEC 17025, laborato...
ISO/IEC 17025:2017, Clause 8.5 & Examples of NC's
Переглядів 4058 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 8.5 - Actions to address risks and opportunities, and examples of nonconformances as per clause 8.5 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/boost/Jobs_Pharma_food_Industry ke...
ISO/IEC 17025:2017, Clause 8.4 , & Examples of NC's
Переглядів 4048 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 8.4 - Control of records, and examples of nonconformances as per clause 8.4 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/boost/Jobs_Pharma_food_Industry keywords: ISO/IEC 17025, l...
ISO/IEC 17025:2017, Clause 8.3 , & Examples of NC's
Переглядів 4108 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 8.3 - Control of management system documents, and examples of nonconformances as per clause 8.3 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/boost/Jobs_Pharma_food_Industry keywor...
ISO/IEC 17025:2017, Clause 8.2 , & Examples of NC's
Переглядів 4008 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 8.2 - Management system documentation, and examples of nonconformances as per clause 8.2 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/Jobs_Pharma_food_Industry keywords: ISO/IEC 1...
ISO/IEC 17025:2017, Clause 8.0 & Clause 8.1
Переглядів 5238 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, clause 8.0 - Management system requirements, and clause 8.1 - Options. Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/Jobs_Pharma_food_Industry keywords: ISO/IEC 17025, laboratory accredit...
ISO/IEC 17025:2017, Clause 7.11, & Examples of NC's
Переглядів 5848 місяців тому
Learn about the requirements of ISO/IEC 17025:2017, Clause 7.11- Control of data and information management, and examples of nonconformances as per Clause 7.11 Join our telegram channel for Pharma, Life Sciences, Food Industries and Laboratory- Jobs, Regulatory updates, Technical updates & add your professional friends or colleagues through this group link t.me/Jobs_Pharma_food_Industry keyword...
ISO/IEC 17025:2017, Clause 7.10, & Examples of NC's
Переглядів 5558 місяців тому
ISO/IEC 17025:2017, Clause 7.10, & Examples of NC's
ISO/IEC 17025:2017, Clause 7.9, & Examples of NC's
Переглядів 5808 місяців тому
ISO/IEC 17025:2017, Clause 7.9, & Examples of NC's
ISO/IEC 17025:2017, Clause 7.8 & Examples of NC's
Переглядів 8778 місяців тому
ISO/IEC 17025:2017, Clause 7.8 & Examples of NC's
ISO/IEC 17025:2017, Clause 7.7 & Examples of NC's
Переглядів 8998 місяців тому
ISO/IEC 17025:2017, Clause 7.7 & Examples of NC's
ISO/IEC 17025:2017, Clause 7.6 & Examples of NC's
Переглядів 5348 місяців тому
ISO/IEC 17025:2017, Clause 7.6 & Examples of NC's
ISO/IEC 17025:2017, Clause 7.5 & Examples of NC's
Переглядів 5938 місяців тому
ISO/IEC 17025:2017, Clause 7.5 & Examples of NC's
ISO/IEC 17025:2017, Clause 7.4 & Examples of NC's
Переглядів 6588 місяців тому
ISO/IEC 17025:2017, Clause 7.4 & Examples of NC's
ISO/IEC 17025:2017, Clause 7.3 & Examples of NC's
Переглядів 6338 місяців тому
ISO/IEC 17025:2017, Clause 7.3 & Examples of NC's
ISO/IEC 17025:2017, Clause 7.2 & Examples of NC's
Переглядів 1,3 тис.8 місяців тому
ISO/IEC 17025:2017, Clause 7.2 & Examples of NC's
ISO/IEC 17025:2017, Clause 7.1 & Examples of NC's
Переглядів 8929 місяців тому
ISO/IEC 17025:2017, Clause 7.1 & Examples of NC's
ISO/IEC 17025:2017, Clause 7.0 - Process requirements
Переглядів 8209 місяців тому
ISO/IEC 17025:2017, Clause 7.0 - Process requirements
ISO/IEC 17025:2017, Clause 6.6 & Examples of NC's
Переглядів 8239 місяців тому
ISO/IEC 17025:2017, Clause 6.6 & Examples of NC's
ISO/IEC 17025:2017, Clause 6.5 & Examples of NC's
Переглядів 8719 місяців тому
ISO/IEC 17025:2017, Clause 6.5 & Examples of NC's
ISO/IEC 17025:2017, Clause 6.4 & Examples of NC's
Переглядів 1,4 тис.9 місяців тому
ISO/IEC 17025:2017, Clause 6.4 & Examples of NC's
ISO/IEC 17025:2017, Clause 6.3 & Examples of NC's
Переглядів 1,1 тис.9 місяців тому
ISO/IEC 17025:2017, Clause 6.3 & Examples of NC's
like
Thank you. It was helpful
@@FaranakBeigmohammadi "Thanks for your feedback! I'm glad you found it helpful.
Superb sir tq it's very nice informative videos ❤
Thanks for your kind words. 🙏
There is no organisation called "I.S.O.". It is the ISO, from the greek word "isos", meaning "the same." The word is pronounced as "eye-so." Your examples are basic, but credible.
Thank you for your valuable comments. 🙏
Thanks for your full explanation and examples of NC.
Thank you.
Great opportunity for learning ISO/IEC-17025:2017