Newsweek
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3 June, 2022
The European system of approval of new medicines comprises an European Union (EU)-wide authorisation procedure (the so called centralised pro- cedure) alongside national procedures based on […]
31 May, 2022
At noon on May 27, 2022, Orioledhub’s birthday party took place in a joyful and warm atmosphere. With the theme of Go Green and the blue […]
16 May, 2022
On the morning of May 14, 2022 in Cao Lanh City, Dong Thap province, Orioled Hub was pleased to participate in the tennis exchange program with […]
23 April, 2022
ORIOLED HUB: TALENT – STRENGTH – RESPONSIBILITY Mission Answering the ‘Why’ question of the organization, also known as the organization’s core purpose and reasons for survival. […]
17 April, 2022
Several important uses of Quality Risk Management in GMP practice Quality Risk Management is increasingly becoming an integral part of an effective pharmaceutical quality system. It […]
8 April, 2022
This is one in a series of guidances that provides recommendations for applicants preparing theCommon Technical Document for the Registration of Pharmaceuticals for Human Use (CTD). […]
3 June, 2022
The European system of approval of new medicines comprises an European Union (EU)-wide authorisation procedure (the so called centralised pro- cedure) alongside national procedures based on […]
31 May, 2022
At noon on May 27, 2022, Orioledhub’s birthday party took place in a joyful and warm atmosphere. With the theme of Go Green and the blue […]
16 May, 2022
On the morning of May 14, 2022 in Cao Lanh City, Dong Thap province, Orioled Hub was pleased to participate in the tennis exchange program with […]
23 April, 2022
ORIOLED HUB: TALENT – STRENGTH – RESPONSIBILITY Mission Answering the ‘Why’ question of the organization, also known as the organization’s core purpose and reasons for survival. […]
17 April, 2022
Several important uses of Quality Risk Management in GMP practice Quality Risk Management is increasingly becoming an integral part of an effective pharmaceutical quality system. It […]
8 April, 2022
This is one in a series of guidances that provides recommendations for applicants preparing theCommon Technical Document for the Registration of Pharmaceuticals for Human Use (CTD). […]