二每年一月向所在地卫生主管机关及管制药品管理局办理前一年第四级管制药品之申报。
Reporting Schedule 4 controlled drugs of the previous year to the local health administration and the NationalBureau of Controlled Drugs in January.
为办理第一级、第二级管制药品之输入、输出、制造及贩卖，管制药品管理局应设立制药工厂为之。
The National Bureau of Controlled Drugs shall establish pharmaceutical plant to handle the import, export, manufacture and selling of the Schedule 1 and 2 controlled drugs.
未于输入凭照、输出凭照期限内办理输入、输出者，应将输入凭照、输出凭照缴回管制药品管理局注销。
If the permit is not used within the set time limit it shall be returned to the National Bureau of Controlled Drugs for cancellation.
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