RESUMO
According to the information of the supervision and inspection of in vitro diagnostic reagents for clinical use, this article analyzed the compliance issues and discussed the methods to solve the problems, to urge medical institutions to reduce the regulatory risk of in vitro diagnostic reagents in use.
Assuntos
Regulamentação Governamental , Indicadores e Reagentes , RiscoRESUMO
OBJECTIVE:To seek for the countermeasures for standardized administration of pharmacy in Chinese hospital.METHODS:The existing problems in pharmacy of Chinese hospital were analyzed.RESULTS & CONCLUSION:Under the current situation of advocating integrated pharmaceutical care,only by strengthening the construction of hardwares and softwares,by establishing the standardized administrative system can we ensure the good quality of drugs and pharmaceutical cares.
RESUMO
OBJECTIVE:To seek for the countermeasures to standardize the administration of medical consultation service in the retail pharmacy.METHODS:To analyse the existing problems of the consultation service in the retail pharmacy.RESULT_S&CONCLUSION:We suggest that the consultation service should be carried out by speciallyassigned persons,CIS should be introduced,computer network should be manipulated and a standardized administration system should be established.Only in this way can the quality of service be raised and the security of medication of the public be ensured.