Shanghai North Carolina passed the "Little Giant" annual acceptance
Release time:
2020-07-31
In order to promote the independent innovation of enterprises, improve the core competitiveness of enterprises, enhance the competitive advantages of enterprises in domestic and foreign industries, and accelerate the construction of scientific and technological innovation, Shanghai North Carolina applied for the Shanghai "Science and Technology Innovation Action Plan" in 2016
87 "Little Giant" cultivation enterprises in Shanghai that year, the project execution period is 2 years. During the period of the Little Giant Cultivation Project, North Carolina completed the re-identification of Shanghai High-tech Enterprises and the identification of Songjiang District Enterprise Technology Center. Songjiang District Enterprise Technology Center was evaluated as excellent, passed the certification of Shanghai Academician Expert Workstation, passed the acceptance of Shanghai Patent Work Pilot Enterprises, and obtained a total of 4
12 invention patents applied, registered trademark 2 , formulated enterprise standard 4 , product inspection report 22 , Songjiang district industry-university-research innovation project in 2017 was approved and completed the project target. Tinib drugs and their intermediates of non-small cell lung cancer (NSCLC
(Cabozantinib) , ceritinib (Ceritinib ) and other kinds of API intermediates for tinib star varieties which are hot spots in the pre-clinical research and development of generic drugs, also focus on the development of palbocicil (Palbociclib ) and gefitinib and other varieties of intermediate production process industrialization pilot and scale-up, and in-depth quality research and factory industrialization practice. In addition, North Carolina has also vigorously expanded the industrialization of the anti-diabetic drug pioglitazone, as well as the development of other products such as the endogenous active substance Paricalcitol, and carried out product layout for future development. During the cultivation project period, North Carolina completed various tasks such as the optimization and construction of the innovation environment, the construction of the research and development team, and the research and development of scientific research projects, and carried out the upgrading and transformation of the research and development laboratory and pilot experiment platform, environmental impact assessment filing and supporting environmental protection treatment facilities. 3# In mid-March, the Shanghai Municipal Science and Technology Commission launched the acceptance and evaluation of Shanghai's science and technology "little giant" enterprises.
enterprises recommended by the Songjiang District Science and Technology Commission participated in the defense. Kang Litao, general manager of Shanghai North Carolina, Li Qian, deputy general manager, and heads of research and development, finance and other departments participated in the on-site defense and successfully passed the defense acceptance. (Yang Shiqiong)
More information
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2020
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Spike New Drug Approved for Registration
On April 16, Jianfeng Pharmaceutical Company received the approval and issuance of Olopatadine Hydrochloride Eye Drops "Drug Registration Approval" (approval number: 2019S00296) approved by the State Drug Administration. Olopatadine hydrochloride eye drops is mainly used to treat the signs and symptoms of allergic conjunctivitis. It is a mast cell stabilizer and a relatively selective histamine H1-receptor antagonist. It can inhibit type I immediate allergic reactions in vivo and in vitro experiments. At present, the product has been included in the "National Basic Medical Insurance, Work Injury Insurance and Maternity Insurance Drug Catalog (2017 Edition)" and classified as Class B. According to the relevant data of IMS database, in 2018, the global sales of olopatadine hydrochloride eye drops were about 0.37 billion US dollars, and the sales in China were about 10.232 million US dollars. Spike Pharmaceuticals already has the corresponding production line, this time to obtain the registration approval, marking Spike Pharmaceuticals has the qualification to carry out the production and sales of olopatadine hydrochloride eye drops, will further enrich the product line of Spike Pharmaceuticals, help to enhance the competitiveness of the company's pharmaceutical business. (Xia Yingpin)
2020
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Spike New Drug Approved for Registration
On April 16, Jianfeng Pharmaceutical Company received the approval and issuance of Olopatadine Hydrochloride Eye Drops "Drug Registration Approval" (approval number: 2019S00296) approved by the State Drug Administration. Olopatadine hydrochloride eye drops is mainly used to treat the signs and symptoms of allergic conjunctivitis. It is a mast cell stabilizer and a relatively selective histamine H1-receptor antagonist. It can inhibit type I immediate allergic reactions in vivo and in vitro experiments. At present, the product has been included in the "National Basic Medical Insurance, Work Injury Insurance and Maternity Insurance Drug Catalog (2017 Edition)" and classified as Class B. According to the relevant data of IMS database, in 2018, the global sales of olopatadine hydrochloride eye drops were about 0.37 billion US dollars, and the sales in China were about 10.232 million US dollars. Spike Pharmaceuticals already has the corresponding production line, this time to obtain the registration approval, marking Spike Pharmaceuticals has the qualification to carry out the production and sales of olopatadine hydrochloride eye drops, will further enrich the product line of Spike Pharmaceuticals, help to enhance the competitiveness of the company's pharmaceutical business. (Xia Yingpin)
2020
07-31