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The State Drug Administration of China recently issued the "14th Five-Year Plan for Drug Regulatory Network Security and Informatization Constructio.
When introducing various key tasks, the "Planning" proposes to realize the comprehensive cloud deployment of business systems, build a "Internet of Things, Data Connection, and Zhilian" digital base for smart drug supervision, and promote the digital transformation and upgrading of drug supervisi.
When introducing various key tasks, the "Planning" proposes to realize the comprehensive cloud deployment of business systems, build a "Internet of Things, Data Connection, and Zhilian" digital base for smart drug supervision, and promote the digital transformation and upgrading of drug supervisi.
The "Plan" proposes that looking forward to the "14th Five-Year Plan" and the long-term goals of 2035, China will realize the leap-forward development from a big pharmaceutical country to a pharmaceutical power, which puts forward higher requirements for the efficiency of drug review and approval and the ability to manage drug safety ris.
The "Plan" pointed out that in the "14th Five-Year Plan" period, the construction of drug supervision informatization should closely focus on the key work of drug supervision, adhere to problem orientation and goal orientation, further promote the in-depth integration of technological innovation and application and the improvement of drug supervision capabilities, and improve the comprehensive supervision efficien.
, improve government service capabilities, and make information technology a key support for promoting the modernization of the drug regulatory system and regulatory capabiliti.
, improve government service capabilities, and make information technology a key support for promoting the modernization of the drug regulatory system and regulatory capabiliti.
Talking about how to strengthen the capacity building of drug supervision, the "Plan" proposes to take the quality supervision of the vaccine production process as a breakthrough, and on the basis of the electronic production and inspection data of vaccine production enterprises , through the research on the data of key links in vaccine production, to explore vaccines Digital production quality management, quality risk early warning and emergency response mechanisms will improve the efficiency of drug supervision and risk management capabiliti.
In terms of the construction of the information traceability system, the "Plan" proposes that the State Administration will continue to strengthen the operation and management of the vaccine traceability collaborative service platform and the national vaccine traceability supervision system, and on this basis, promote the construction of the drug information traceability system, and establish and improve the drug traceability syst.
, expand the construction of a drug traceability collaborative service platform and traceability supervision system, and gradually realize the supervision of the traceability of key varieties such as narcotic drugs, psychotropic drugs, blood products, and the varieties selected by the state's centralized procuremen.
, expand the construction of a drug traceability collaborative service platform and traceability supervision system, and gradually realize the supervision of the traceability of key varieties such as narcotic drugs, psychotropic drugs, blood products, and the varieties selected by the state's centralized procuremen.
In terms of building a solid digital base for smart drug supervision, the "Planning" also proposes that starting from the actual needs of drug supervision work, on the basis of the existing information construction achievements, through "new infrastructure" to empower the innovation and development of supervision business, optimize and improve drugs Supervision informatization standard system, promote the in-depth application of cloud technology, improve the support and service capabilities of the drug supervision cloud platform, realize the comprehensive cloud deployment of business systems, and build a solid digital foundation for the "Internet of Things, Data Connection, and Zhilian" drug smart supervision, promote Digital transformation and upgrading of drug supervisi.
(Finish)
(Finish)
The State Drug Administration of China recently issued the "14th Five-Year Plan for Drug Regulatory Network Security and Informatization Constructio.
When introducing various key tasks, the "Planning" proposes to realize the comprehensive cloud deployment of business systems, build a "Internet of Things, Data Connection, and Zhilian" digital base for smart drug supervision, and promote the digital transformation and upgrading of drug supervisi.
When introducing various key tasks, the "Planning" proposes to realize the comprehensive cloud deployment of business systems, build a "Internet of Things, Data Connection, and Zhilian" digital base for smart drug supervision, and promote the digital transformation and upgrading of drug supervisi.
The "Plan" proposes that looking forward to the "14th Five-Year Plan" and the long-term goals of 2035, China will realize the leap-forward development from a big pharmaceutical country to a pharmaceutical power, which puts forward higher requirements for the efficiency of drug review and approval and the ability to manage drug safety ris.
The "Plan" pointed out that in the "14th Five-Year Plan" period, the construction of drug supervision informatization should closely focus on the key work of drug supervision, adhere to problem orientation and goal orientation, further promote the in-depth integration of technological innovation and application and the improvement of drug supervision capabilities, and improve the comprehensive supervision efficien.
, improve government service capabilities, and make information technology a key support for promoting the modernization of the drug regulatory system and regulatory capabiliti.
, improve government service capabilities, and make information technology a key support for promoting the modernization of the drug regulatory system and regulatory capabiliti.
Talking about how to strengthen the capacity building of drug supervision, the "Plan" proposes to take the quality supervision of the vaccine production process as a breakthrough, and on the basis of the electronic production and inspection data of vaccine production enterprises , through the research on the data of key links in vaccine production, to explore vaccines Digital production quality management, quality risk early warning and emergency response mechanisms will improve the efficiency of drug supervision and risk management capabiliti.
enterprise enterprise enterpriseIn terms of the construction of the information traceability system, the "Plan" proposes that the State Administration will continue to strengthen the operation and management of the vaccine traceability collaborative service platform and the national vaccine traceability supervision system, and on this basis, promote the construction of the drug information traceability system, and establish and improve the drug traceability syst.
, expand the construction of a drug traceability collaborative service platform and traceability supervision system, and gradually realize the supervision of the traceability of key varieties such as narcotic drugs, psychotropic drugs, blood products, and the varieties selected by the state's centralized procuremen.
purchase purchase purchase, expand the construction of a drug traceability collaborative service platform and traceability supervision system, and gradually realize the supervision of the traceability of key varieties such as narcotic drugs, psychotropic drugs, blood products, and the varieties selected by the state's centralized procuremen.
In terms of building a solid digital base for smart drug supervision, the "Planning" also proposes that starting from the actual needs of drug supervision work, on the basis of the existing information construction achievements, through "new infrastructure" to empower the innovation and development of supervision business, optimize and improve drugs Supervision informatization standard system, promote the in-depth application of cloud technology, improve the support and service capabilities of the drug supervision cloud platform, realize the comprehensive cloud deployment of business systems, and build a solid digital foundation for the "Internet of Things, Data Connection, and Zhilian" drug smart supervision, promote Digital transformation and upgrading of drug supervisi.
(Finish)
Standard Standard Standard Drug _ _ (Finish)
