Medical device unique identification database constitutes an important part of the medical device unique identification system. In accordance with the requirements of theRules for Unique Identificatio
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To implement the Regulations on Optimizing the Business Environment in China, NMPA and the General Administration of Customs have collaboratively established a management system for import filing of p
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Updated: 2019-11-29 On November 29, 2019, NMPA issued the Announcement on Issues Pertaining to the Implementation of the Drug Administration Law of the People's Republic of China (2019 No. 103)
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According to the newly revised Drug Administration Law of the People's Republic of China, drug clinical trial institutions shall be subject to record filing management in lieu of accreditation. NM
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The BMA survey shows that the majority of doctors think ambitions to get the NHS back to near-normal service by autumn are unlikely to be realised, highlighting the sheer scale of the challenge of tac
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For Immediate Release:July 09, 2020The U.S. Food and Drug Administration today announced the following actions taken in its ongoing response effort to the COVID-19 pandemic:Today, a U.S. District Cour
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For Immediate Release:July 02, 2020 Today, the U.S. Food and Drug Administration approved Rukobia (fostemsavir), a new type of antiretroviral medication for adults living with HIV who have tried multi
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For Immediate Release:July 02, 2020 Today, the U.S. Food and Drug Administration further assisted health care providers around the country prepare for the upcoming flu season during the COVID-19 pande
2020-07-10 vcc 24