The 2022 (8th) China Pharmaceutical Trade Annual Conference will be held in Guangzhou from November 22 to 23, 2022.
On July 25, the State Food and drug administration, in accordance with the relevant provisions of the drug administration law and the special drug approval procedures, carried out emergency review and approval, and conditionally approved the application for registration of azvudine tablets of Henan Zhenzhen Biotechnology Co., Ltd. to increase the indications for treatment of novel coronavirus pneumonia.
The 2021 annual drug evaluation report shows that the drug administration department is committed to building a scientific, authoritative and open evaluation standard system. 87 guiding principles were issued in 2021, and a total of 361 guiding principles have been issued, covering traditional Chinese medicine, chemical drugs, biological products and other fields, including hot and difficult issues such as novel coronavirus therapeutic drugs, ancient classic prescriptions, cells and gene therapy, It provides scientific and powerful technical support for the innovative development of the pharmaceutical industry and drug evaluation.
《The 2021 annual drug review report 》shows that the breakthrough treatment drug procedure, conditional approval procedure,priority review and approval procedure, and special approval procedure. Four "fast channels 'help accelerate drug research and development and marketing.
Recently, the Guangdong Provincial Food and Drug Administration has integrated the province's drug testing technical resources, with the provincial drug testing institute as the leader, coordinating the drug testing agencies in various cities, establishing a green channel for drug testing involved, and providing efficient and fast testing technology support for drugs and cosmetics involved, better Cooperate with the public security department to do a good job in the inspection and identification of cases involved, and improve the quality and efficiency of special rectification work.
The draft revision of the Implementation Regulations of the Drug Administration Law for comments has a total of 181 articles in ten chapters and nearly 30,000 words. The legal provisions were refined, the supervision and management measures were improved, the connection between executions was added, supervision support was strengthened, and further regulations were made on the production, operation and supply guarantee of drugs. In particular, there are clear regulations on the production management of Chinese herbal decoction pieces and formula granules, and the management of drug online sales.