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Notice of the State Food and Drug Administration on the Publication of the Catalogue of Generic Drug Reference Preparations (46th Batch) (No. 82 [2021
Time of Update: 2022-10-01
doc to Notice No. 82 [2021] of the State Drug Administration After the review and confirmation of the Expert Committee on the Consistency Evaluation of Generic Drugs and Efficacy of the State Drug Administration, the Catalogue of Generic Drug Reference Preparations (46th Batch) is hereby published.
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The domestic antibacterial drug market has entered the market again, and it is predicted that the next 8 years may show a trend of first rising and then falling
Time of Update: 2022-09-06
【Pharmaceutical Network Market Analysis】 In the field of steady growth of antibacterial drugs, the author learned that a pharmaceutical company has recently ushered in.
【Pharmaceutical Network Market Analysis】 In the field of steady growth of antibacterial drugs, the author learned that a pharmaceutical company has recently ushered in.
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Nature: Mushroom toxin increases brain connections, treats severe depression
Time of Update: 2022-05-23
The study shows that psilocybin, a hallucinogen that occurs naturally in some hallucinogenic mushrooms, is able to respond to treatment in patients with treatment-resistant depression by increasing functional network connections in the brain .
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Omicron Variant New Coronavirus Inactivated Vaccine Approved to Enter Clinical Trials
Time of Update: 2022-05-14
Yang Xiaoming, chief engineer of Sinopharm Group and chairman of Sino Bio, introduced that according to the guidelines and research and development strategies of the improved new crown vaccine of the State Food and Drug Administration, since December 9, 2021, the research and development of the new coronavirus inactivated vaccine of the Omicron variant strain has been launched.
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Exquisite jade pen, flowers all the way - Quanxinda® (ofatumumab) brings new hope to "beauty disease
Time of Update: 2022-04-27
In the second year of ofatumumab treatment, nearly 90% of patients achieved the composite index of no recurrence, no new or enlarged lesions, and no disability progression-NEDA-3 (no evidence of disease activity) [4] .
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Pfizer's Oral Covid-19 Drug Paxlovid Receives FDA Emergency Use Authorization
Time of Update: 2022-02-24
S. Food and Drug Administration (FDA) has approved an Emergency Authorization Application (EUA) for its novel COVID-19 oral antiviral drug candidate Paxlovid for the treatment of non-hospitalized adults with COVID-19 infection at high risk of developing severe disease .
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19 new Class 1 drugs were added this week, and 6 clinical trials in the field of domestic oncology drugs were approved
Time of Update: 2021-12-24
(People's Daily Health Client Li Xuanzhang) As of December 11, 2021, data from the Center for Drug Evaluation (CDE) of the China National Medical Products Administration shows that a total of 5,980 clinical trial applications have passed "implicit permission .
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The Comprehensive Department of the State Food and Drug Administration publicly solicits opinions on the "Measures for the Supervision and Administration of Drug Operation and Use Quality
Time of Update: 2021-12-01
The "Measures for the Supervision and Administration of Drug Operation and Use Quality" have been revised and perfected and are now again open to the public for comments .
cn via e-mail before November 26, 2021, and the subject of the email should indicate "Feedback on Drug Operation and Use Measures" .
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The State Food and Drug Administration participates in the 2021 committee meeting of the Drug Inspection Cooperation Plan
Time of Update: 2021-11-02
On October 26, the official website of the State Food and Drug Administration announced that on October 19, 2021, the State Food and Drug Administration participated in the 2021 Committee Meeting of t
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A surprising discovery reveals a rare cause of epilepsy
Time of Update: 2021-08-03
Victor Anggono of the University of Queensland Brain Research Institute said that his team made a breakthrough discovery when studying nerve cell communication, which is an important process for normal brain function .
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CDE issued a notice of "Technical Guidelines for the Evaluation of Similarity of Biosimilars and the Extrapolation of Indications
Time of Update: 2021-07-26
Announcement of the Center for Drug Evaluation of the National Food and Drug Administration on Issuing the Technical Guidelines for Similarity Evaluation and Indication Extrapolation of Biosimilar Drugs (No.
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Announcement of the State Food and Drug Administration on the conversion of Banlangen chewable tablets to over-the-counter drugs (No. 130 of 2020
Time of Update: 2021-07-07
The contents of the non-prescription drug inserts other than those specified in the template inserts shall be implemented in accordance with the original approval documents .
Templates for non-prescription drug instructions State Food and Drug Administration November 23, 2020 Announcement No.
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Sinopharm's new crown vaccine obtains emergency use license from Thailand's Food and Drug Administration
Time of Update: 2021-06-30
It was reported on May 28 that a senior official from the Thai health department stated that the Thai Food and Drug Administration approved an emergency use license for the new crown vaccine developed by China National Pharmaceutical Group on the 28th .
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Haisco medium and long chain fat emulsion/amino acid (16)/glucose (16%) injection review
Time of Update: 2021-06-02
The long-chain fat emulsion/amino acid (16)/glucose (16%) injection developed by the generic drug product obtained the drug registration approval issued by the National Medical Products Administration in July 2018 (batch number: 2018S00429).
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Weihai City Market Supervision Bureau released the results of food sampling inspections
Time of Update: 2021-05-20
html" class="zdbq" title="Sugar-related food information" target="_blank">21250，、24。 、 The pipi shrimp (seawater product) and cadmium (calculated as Cd) sampled at Xiaoguo Aquatic Products Store in Torch High-tech Industrial Development Zone, Weihai do not meet the national food safety standards.
