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| State Food and Drug Administration issued "2010 drug production and management supervision plan" |
To strengthen supervision of pharmaceutical production and trading sectors, recently, the State Food and Drug Administration issued the "2010 Plan pharmaceutical production supervision" and "Drug Supervision in 2010, the work plan."
"The 2010 work plan for monitoring drug production" requirement, one day supervision and management of medicine production; Second, overall pharmaceutical GMP certification inspection; third is to strengthen supervision of production of essential drugs; Fourth, the implementation of drug safety in all aspects related to drug production task requirements; 5 is to strengthen the supervision of vaccine production; sixth is to strengthen the special drug administration; 7 is part of pharmaceutical production and do a good job of implementation of electronic monitoring code; eight is to strengthen the monitoring of adverse drug reactions and the re-evaluation; 9, continue to medicine injection and then evaluation.
"Drug Supervision in the 2010 work plan" requirement, One is to strengthen the drug management aspects of daily supervision and inspection work; Second, the implementation of drug safety aspects involved in the pharmaceutical business of the job requirements; third is to strengthen business links to essential medicines supervision and management; Fourth, do the "Two Networks", to promote the demonstration counties to create drug safety activities; 5 is earnestly drugs operation code part of the implementation of electronic monitoring; sixth is to strengthen supervision and management of drug use areas; 7 is effective good vaccine management supervision; 8 is to carry out the work of pharmaceutical business credit system.
State Food and Drug Administration requires all levels of food and drug supervision department under the 2010 Drug Supervision in the production and deployment work Jihua, strengthen organization and leadership, the full implementation of regulatory responsibility, earnestly perform their duties, to establish cooperation mechanisms and long-term mechanism, strengthen the supervision and inspection and report information in a timely manner, good production and business aspects of drug safety supervision, strengthen the management of the daily supervision of medicine production, intensify and improve the efficiency of supervision, to ensure drug safety. |
| AddTime：2010-5-27 16:46:24 |
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