The State Council clarifies the twelve and 7 tasks through the national pharmaceutical safety plan
Release time: 2011-12-09 & nbsp & nbsp & nbsp Source:
According to the China Government Network News，Premier of the State Council hosted the Executive Meeting of the State Council on the 7th，Discussion passed the "National Drug Safety Plan (2011-2015)"。
Meeting to point out，Current，China has formed a relatively complete pharmaceutical production and supply system，Basic establishment of coverage of drug development、Production、The safety supervision system of circulation and use the whole process，Drug safety status has improved significantly，Drug safety guarantee capabilities have improved significantly。but，Increased My stake betting appstake online sports bettingintegrity system for pharmaceutical companies、The weak regulatory power and weak technical support system are relatively prominent，Drug safety is still at a high risk period。We must adhere to safety first、Principles of scientific supervision，Implementation of drug safety liability，Improve regulatory efficiency，Make sure the quality of the medicine，Comprehensively improving drug safety guarantee capabilities，Reduce drug safety risk。
The "National Drug Safety Plan" discussed the meeting discussed the overall goal and key tasks of drug safety work during the "Twelfth Five -Year Plan" period。until 2015，Pharmaceutical production 100%meets the requirements of the newly revised "Management of Drug Production Quality Management" requirements，The level of drug safety has increased significantly，The safety satisfaction of the people's medication is significantly improved。
The key task is:
(1) Improve national standards。Strive for chemical medicine、Biological product standards are in line with international standards，Traditional Chinese Medicine Standard Leading International Standards。
(2) Improve the inspection and detection system。Strengthen the construction of a national pharmaceutical inspection institution，Improvement province、Di (City) -level institutional laboratory condition，Strengthen the construction of the fast inspection capacity of county -level institutions。
stake online sports bettingstake betting app(3) Enhanced quality management of the entire process of strengthening drugs and medical equipment。Improve the development of drugs，Promote integration with international standards。Improve clinical trial site supervision and inspection coverage。Establish a traceability system for the circulation of Chinese medicinal materials，Promote the standardized production of commonly used Chinese medicinal materials。Accelerate the construction of supervision informatization，Uniform encoding management for the approved listed drugs，Electronic supervision covers all drug varieties。
(4) Strengthen safety monitoring and early warning。Comprehensive adverse reactions and drug abuse monitoring system，Improve the system after the drug is listed，Key strengthening new drugs、Chinese medicine injection、Safety monitoring and evaluation of high -risk drugs。perfect emergency plan，Ensure that emergency drugs are supplied in a timely manner。
(5) Improve the capacity of basic drug production in the country，Make sure quality and safety、Fairness and。Strengthen basic drug drawing and bidding、Purchasing、Use quality management，Improve the basic drug supply network and supervision network。
(6) Establish a long -term mechanism for drug safety supervision。Improve the price of drug price formation、Concentrated procurement policy and pharmaceutical drawing work mechanism，Improve the System of Recall and stake sports betting appstake sports betting appDisposal of Drugs and Purchase Drugs。Evaluation of credit rating of pharmaceutical companies，Establish a corporate integrity file，Patients with serious violations、Trusting person implements industry ban。Strict cracking down on the production and sale of counterfeit and inferior drugs。
(7) Deepen reform，Improve the legal system。Deepen the reform of the administrative approval system of drugs，Strict standard，Specification Program。Innovative drug law enforcement system mechanism，Strengthen law enforcement supervision。Standardize the order of drug circulation，Reduce circulation link。Accelerate the revision of the relevant laws and regulations。
The meeting requests to follow the responsibility of the local government、The regulatory authorities are responsible for their responsibility、Enterprise is the requirements of the first responsible person，Implementation of drug safety liability，Strengthen departmental collaboration and joint law enforcement。Strengthen publicity and education，Improve the public safety medication、Reasonable consciousness of medication。Strengthen talent、Technology and investment support，Promoting adjustment of the pharmaceutical industry structure，Improve independent innovation ability。
The meeting requests to follow the responsibility of the local government、The regulatory authorities are responsible for their responsibility、Enterprise is the requirements of the first responsible person，Implementation of drug safety liability，Strengthen departmental collaboration and joint law enforcement。Strengthen publicity and education，Improve the public safety medication、Reasonable consciousness of medication。Strengthen talent、Technology and investment support，Promoting adjustment of the pharmaceutical industry structure，Improve independent innovation ability。
Meeting to point out，Current，China has formed a relatively complete pharmaceutical production and supply system，Basic establishment of coverage of drug development、Production、The safety supervision system of circulation and use the whole process，Drug safety status has improved significantly，Drug safety guarantee capabilities have improved significantly。but，Increased My stake betting appstake online sports bettingintegrity system for pharmaceutical companies、The weak regulatory power and weak technical support system are relatively prominent，Drug safety is still at a high risk period。We must adhere to safety first、Principles of scientific supervision，Implementation of drug safety liability，Improve regulatory efficiency，Make sure the quality of the medicine，Comprehensively improving drug safety guarantee capabilities，Reduce drug safety risk。
The "National Drug Safety Plan" discussed the meeting discussed the overall goal and key tasks of drug safety work during the "Twelfth Five -Year Plan" period。until 2015，Pharmaceutical production 100%meets the requirements of the newly revised "Management of Drug Production Quality Management" requirements，The level of drug safety has increased significantly，The safety satisfaction of the people's medication is significantly improved。
The key task is:
(1) Improve national standards。Strive for chemical medicine、Biological product standards are in line with international standards，Traditional Chinese Medicine Standard Leading International Standards。
(2) Improve the inspection and detection system。Strengthen the construction of a national pharmaceutical inspection institution，Improvement province、Di (City) -level institutional laboratory condition，Strengthen the construction of the fast inspection capacity of county -level institutions。
stake online sports bettingstake betting app(3) Enhanced quality management of the entire process of strengthening drugs and medical equipment。Improve the development of drugs，Promote integration with international standards。Improve clinical trial site supervision and inspection coverage。Establish a traceability system for the circulation of Chinese medicinal materials，Promote the standardized production of commonly used Chinese medicinal materials。Accelerate the construction of supervision informatization，Uniform encoding management for the approved listed drugs，Electronic supervision covers all drug varieties。
(4) Strengthen safety monitoring and early warning。Comprehensive adverse reactions and drug abuse monitoring system，Improve the system after the drug is listed，Key strengthening new drugs、Chinese medicine injection、Safety monitoring and evaluation of high -risk drugs。perfect emergency plan，Ensure that emergency drugs are supplied in a timely manner。
(5) Improve the capacity of basic drug production in the country，Make sure quality and safety、Fairness and。Strengthen basic drug drawing and bidding、Purchasing、Use quality management，Improve the basic drug supply network and supervision network。
(6) Establish a long -term mechanism for drug safety supervision。Improve the price of drug price formation、Concentrated procurement policy and pharmaceutical drawing work mechanism，Improve the System of Recall and stake sports betting appstake sports betting appDisposal of Drugs and Purchase Drugs。Evaluation of credit rating of pharmaceutical companies，Establish a corporate integrity file，Patients with serious violations、Trusting person implements industry ban。Strict cracking down on the production and sale of counterfeit and inferior drugs。
(7) Deepen reform，Improve the legal system。Deepen the reform of the administrative approval system of drugs，Strict standard，Specification Program。Innovative drug law enforcement system mechanism，Strengthen law enforcement supervision。Standardize the order of drug circulation，Reduce circulation link。Accelerate the revision of the relevant laws and regulations。
The meeting requests to follow the responsibility of the local government、The regulatory authorities are responsible for their responsibility、Enterprise is the requirements of the first responsible person，Implementation of drug safety liability，Strengthen departmental collaboration and joint law enforcement。Strengthen publicity and education，Improve the public safety medication、Reasonable consciousness of medication。Strengthen talent、Technology and investment support，Promoting adjustment of the pharmaceutical industry structure，Improve independent innovation ability。
The meeting requests to follow the responsibility of the local government、The regulatory authorities are responsible for their responsibility、Enterprise is the requirements of the first responsible person，Implementation of drug safety liability，Strengthen departmental collaboration and joint law enforcement。Strengthen publicity and education，Improve the public safety medication、Reasonable consciousness of medication。Strengthen talent、Technology and investment support，Promoting adjustment of the pharmaceutical industry structure，Improve independent innovation ability。
