06.09.2023
What is SA 8000? SA 8000 Requirements for Businesses
SA 8000 is a system of social accountability standards designed to improve working conditions for employees.
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12.07.2022
3 reasons for unqualified cleanliness in GMP cleanrooms
Getting GMP certification is not an easy task. This article will list 3 main reasons for unqualified cleanliness in GMP cleanrooms. Let's find out! When the GMP cleanroom is tested, there are often some cases where the cleanliness test fails. It could be
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12.07.2022
What Is Operating Cleanroom Class 100, 1000, 10000?
The advent of clean operating room has become a major revolution in the development of the operating room. Laminar airflow operating room air cleanliness can be divided into Class 100 cleanroom, class 1000 cleanroom, class 10 000 cleanroom, class 100 000
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12.07.2022
Class A, class B, class C, class D cleanroom
What is class A, class B, class C, class D cleanroom? Vietnam Cleanroom will answer the question in this article. Let’s find out! 1. Cleanroom classification Class A, class B, class C, class D cleanroom refer to cleanroom cleanliness requirements for
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12.07.2022
What Is ISO 8, ISO 7, ISO 6, ISO 5 Cleanroom?
Cleanrooms are classified by how clean the air inside them is. Cleanroom class is the level of cleanliness the room has. What is ISO 8, ISO 7 cleanroom? It depends on the number of particles found in the room' air. Let's find out with VCR.
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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
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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
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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
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12.07.2022
What is GMP?
What is GMP and how does it relate to pharmaceuticals? How to practice GMP? What are the popular GMP standards in the world? We often see signs in medicines that say
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12.07.2022
Why GMP is crucial to supplement industry?
The supplement industry is big business. In Vietnam, the industry is worth over 5 billion per year and is still growing. As the decades have progressed, the supplement industry has evolved from chalky calcium tablets and foul-smelling cod liver oil, to an
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Comparing Airflow Standards: ISO 14644 vs ASHRAE
Wednesday, 01/10/2025 | 17:16 -
When should WHO-GMP be used instead of EU-GMP?
Wednesday, 01/10/2025 | 16:31
