Newsweek
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5 January, 2023
At present, technology transfer in general, and transfer analytical method, in particular, is a problems of great concern for factories or laboratories. The transfer of analytical […]
30 December, 2022
An orphan drug designation is a status delivered by FDA (US) or EMA (Europe) for pharmaceutical drug that has been developed specifically to treat an ultra-rare […]
14 December, 2022
Overview Patient safety is the primary objective of the Pharmaceutical Quality System (PQS), Manufacturing Authorization holder is required to manufacture safe and effective medicinal products in […]
24 November, 2022
On the morning of November 24, the Workshop on “Exchange of experience in upgrading the quality system of a pharmaceutical production facility to EU – GMP […]
22 November, 2022
Last week, with the excitement of the trainees, the training course “Overview of Pharmacy” hosted by OHI Research Institute ended with hot certificates given to each […]
7 November, 2022
1. Background of GMP In the United States in the early 20th century when the industry was still aboriginal (ice was used for refrigeration, and milk […]