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12.07.2022

Six sigma application in pharma industry

1.What is 6 sigma? 6 sigma is a methodology that helps companies eleminate defects and improve business process, thereby boosting their products quality and profits. It was developed by Motorola with the aim of achieveing fewer defects in parts

12.07.2022

ISO 14644 cleanroom standards

For many manufacturing or research activities, pollution control is very important. Through the clean room environment (clean room) environmental management and strict process control, so that pollution control easier. This ISO 14644 clean room standards

12.07.2022

Data Integrity Principles In Pharmaceutical Industry

Data integrity is one of the most important requirements in the pharmaceutical industry. It especially refers to Chapter 4 of the EU GMP. Recently, the issue of data integrity in these industries is becoming a hot topic among regulators and pharmaceutical

12.07.2022

Good Laboratory Practices (GLP)

GLP about Methods, Personnel, Instruments/Equipment, Dilutions, Weighing, Mobile phase preparation, HPLC and Column care

12.07.2022

ISO 6 - Class 1000 clean room

Cleanrooms are classified based on the number of particles found in the air. In this article, VCR will provide information about a type of cleanroom - Class 1000 cleanroom or ISO 6 clean room 1. What is class 1000 cleanroom - iso class 6 clean room? Class

12.07.2022

What is class 100 000 cleanroom?

Cleanrooms are classified based on the number of particles found in the air. In this article, VCR will provide information about a type of cleanroom - Class 100 000 cleanroom or ISO 8 clean room

12.07.2022

ISO 7 class 10000 cleanroom definition

Cleanrooms are classified based on the number of particles found in the air. In this article, VCR will provide information about a type of cleanroom - Class 10000 cleanroom or ISO 7 clean room 1. What is class 10000 cleanroom - iso class 7 clean room?