GMP-WHO is a very familiar term, as well as a mandatory standard in the field of pharmaceutical manufacturing. So what is the GMP-WHO standard? What criteria does a pharmaceutical manufacturer that wants to meet the GMP-WHO standard have? Let’s find out with GMP Groups in the article below.

Good manufacturing practices (GMP) are one of the sets of principles and standards to be ensured for pharmaceutical production facilities. In the trend of global integration, Vietnamese production facilities not only need to meet domestic requirements but also comply with the requirements of other regions and territories such as GMP-EU, GMP-WHO, GMP-Japan standards. In this article, let’s find out what the GMP-EU standard is. How is GMP-EU different from GMP-WHO?

ISO 13485 is widely applied to medical device manufacturers. This is also a requirement if the manufacturing facility of medical instruments, medical devices, medical supplies wants its products to be widely recognized globally. The current version of ISO 13485 is ISO 13485:2016. What is ISO 13485? What are the benefits of applying ISO 13485 and which unit advises on prestigious standards? Join GMP Groups to find out in the following content.

Any product before launching to the market must pass quality control and meet GLP standards. Let’s see what the GLP standard is with GMP Groups. What requirements do GLP-standard laboratories meet!