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BioWorld - Wednesday, April 29, 2026
Home » Topics » Regulatory » NMPA

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China NMPA grants conditional approval to toripalimab in nasopharyngeal carcinoma

Feb. 22, 2021

Sinovac COVID-19 vaccine gets approved in China; doors opening elsewhere

Feb. 9, 2021
By David Ho and Gina Lee
HONG KONG – Sinovac Biotech Ltd.’s COVID-19 vaccine, Coronavac, received conditional approval for use by the general public from China’s National Medical Productions Administration (NMPA), two days after filing for conditional market authorization.
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Sinovac's CoronaVac COVID-19 vaccine granted conditional marketing authorization in China

Feb. 9, 2021

Sinovac COVID-19 vaccine gets approved in China; doors opening elsewhere

Feb. 8, 2021
By David Ho and Gina Lee
HONG KONG – Sinovac Biotech Ltd.’s COVID-19 vaccine, Coronavac, received conditional approval for use by the general public from China’s National Medical Productions Administration, two days after filing for conditional market authorization.
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Tyvyt approved in China for first-line nonsquamous NSCLC

Feb. 3, 2021

Chinese approval of Rykindo for schizophrenia and psychotic states

Jan. 15, 2021

Tislelizumab approved in China for first-line advanced squamous NSCLC

Jan. 14, 2021

Phase III trial of sacituzumab govitecan in metastatic urothelial cancer cleared to begin in China

Jan. 7, 2021

Chi-Med wins China approval for first in-house oncology drug

Jan. 5, 2021
By David Ho
HONG KONG – Hutchison China Meditech Ltd. (Chi-Med) earned approval from China’s National Medical Products Administration (NMPA) for Sulanda (surufatinib) for the treatment of non-pancreatic neuroendocrine tumors (NETs).
Read More

Sinopharm CNBG's COVID-19 vaccine approved in China

Jan. 5, 2021
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