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5 January, 2023

Transfer Of Analytical Methods Between Two Units And Laboratories

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

Orphan Drug Designation

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

Pharmaceutical Quality System (PQS)

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

Workshop On “Exchange Of Experience In Upgrading The Quality System Of A Pharmaceutical Production Facility To EU – GMP Standards” By OrioledHub And Equilab

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

Internal Training Course On Pharmaceutical Overview For Non-Pharmaceutical Staff

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

Overview Of GMP

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 […]

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5 January, 2023

Transfer Of Analytical Methods Between Two Units And Laboratories

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

Orphan Drug Designation

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

Pharmaceutical Quality System (PQS)

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

Workshop On “Exchange Of Experience In Upgrading The Quality System Of A Pharmaceutical Production Facility To EU – GMP Standards” By OrioledHub And Equilab

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

Internal Training Course On Pharmaceutical Overview For Non-Pharmaceutical Staff

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

Overview Of GMP

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 […]
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