Pharmaceutical companies organize learning of the new "safety production law"
Release time:
2021-09-13
News from our newspaper # On the morning of February 26 , the pharmaceutical company organized department managers, deputy managers and supervisors to study the new "Safety Production Law.
2021version of the "production safety law" has been implemented since 2021 9 1 , with a total of 119 articles. compared with 2014 version, 57 articles have been revised. The new version of the "Safety Production Law" puts forward for the first time that safety production work should adhere to the leadership of the Communist Party of China, should be people-oriented, adhere to the people first, life first, put the protection of people's lives and safety in the first place, and prevent and resolve major safety risks from the source. new ideas. According to the actual situation of the enterprise, the pharmaceutical company has emphatically interpreted the implementation of "industry must be in charge of safety, business must be in charge of safety, production and operation must be in charge of safety " ; Establish and improve the responsibility system for safe production and the rules and regulations for safe production, strengthen the standardization and information construction of safe production, and build a dual prevention mechanism for safety risk classification control and hidden danger investigation and management; high-risk industry areas to insure safety production liability insurance and other provisions. At the study meeting, the amendments to the seven responsibilities of the main responsible person and safety management personnel in production safety management were also interpreted one by one. At the
meeting, Huang Jinlong, deputy general manager of the group company and general manager of the pharmaceutical company, asked all subordinate enterprises to seriously study the new safety law, so as to know, understand and act in accordance with the law. Improve the responsibility system for production safety, vertically to the end, horizontally to the edge, layer by layer compaction responsibility; Establish and improve the dual prevention mechanism, strengthen risk identification and hidden danger investigation, and increase the assessment of hidden danger rectification; Increase the investment in human, ensure that professional management personnel are in place, funds are in place, equipment implementation and protective equipment are in place; strengthen education and training, improve the operability of emergency plans and organize emergency drills; comprehensively implement the construction of safety production standardization, further improve various rules and regulations, and strictly implement them. After the
meeting, subordinate units and departments such as the pharmaceutical company, the new peak north card, and the production department of the pharmaceutical company also organized their employees to study the contents of the new "safe production law.
(Song Shijie)
More information
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2020
07-31
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
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