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State Drug Administration: In 2013
Release time: 2013-02-07 & nbsp & nbsp & nbsp Source: Anonymous

    According to the website of the State Food and Drug Administration,The National Food and Drug Administration issued a notice a few days ago,Requires the relevant work of the electronic supervision of imported drugs。
 
In order to implement the State Food and Drug Administration's "Notice on Printing and Distributing 2011-2015 Pharmaceutical Electronic Supervision Work Plan" (National Food and Drug Administration Office [2012] No. 64) and other relevant work requirements,A few days ago,The State Food and Drug Administration issued notifications on the implementation of electronic supervision of imported drugs。
 
Notification to point out,Overseas Pharmaceutical Manufacturers (that is, "Import Drug Registration stake betting appstake sports betting appCertificate" or "Medical Product Registration Certificate" & ldquo; Company Name & RDQUO; Enterprise) In response to its general responsibility for the implementation of electronic supervision implementation to my country for drugs,Implement drug electronic supervision according to the specified varieties and periods stipulated in the State Food and Drug Administration,and should designate a pharmaceutical manufacturer in my country、Drug Wholesale Enterprise、The subsidiaries or offices established in the territory,Agent agency (hereinafter referred to as electronic supervision agency)。Overseas pharmaceutical manufacturers shall authorize its electronic supervision agency as a fixed contact unit for the drug supervision and management department and related institutions in my country,Assisting it to handle the implementation of drugs and electronic supervision in the country,can assist overseas factories to apply for electronic supervision code、Data upload and related drug recalls。
 
Notification emphasis,Overseas pharmaceutical manufacturers shall, in accordance with the State Food and Drug Administration's "Guiding Opinions of the Drug Electronics Supervision Work" and "Guidance Opinions of the Technical Guidance of Drug Electronics Supervision" requesting the implementation of imported drugs and electronic supervision。Code work (including the establishment of the relationship between the establishment of drug packaging at all levels) should be completed stake online sports bettingin Stake Sports Bettingthe production plant or packaging factory stated in the imported drug registration certificate。Get approved varieties of packaging in the country,Pay code in the approved sub -packaging enterprise。It is forbidden to be unpacking code for the large packaging product in other places。Due to Internet communication and other problems,When visiting China Pharmaceutical Electronics Regulatory Network is difficult,It can be entrusted to the electronic regulatory agency to apply for an electronic regulatory code,Upload the code、Related relationship data and drugs enter the warehouse、Data from the warehouse,Calculate the verification verification。The imported drugs that should be implemented by electronic supervision should be implemented before December 31, 2013,Its electronic regulatory agency shall submit a report before February 28, 2013,and add relevant institutions to China Pharmaceutical Electronic Supervision Network。I have entered the Internet imported enterprise before,It should also make up for the required information in accordance with the requirements of the "Import Drug Enterprise Entry Registration Form"。Newly added national and local basic drugs after January 1, 2013,Its overseas pharmaceutical manufacturers do not designate the electronic regulatory agency shall be specified in time,and report information according to the requirements of this notice、Apply for network access registration,Complete the code for the relevant imported Stake Sports Bettingdrugs stake online sports bettingwithin 12 months after the release of the new directory,and carry out nuclear sales and other tasks。。
 
Notification requirements,Provincial drug supervision and administration departments shall be publicly opened the list of imported drugs and electronic supervision agencies and imported drug data,All imported drugs registered by the agency and the agency of the agency and the agent of the agent are included in the scope of the implementation of the drug electronic supervision and supervision supervision and supervision of the agency,Training for electronic supervision agency、Guidance,Understand its overseas pharmaceutical manufacturers according to the prescribed time limit、Variety and requirements to complete electronic supervision related work。It shall be ordered to correct the case of breeding codes in violation of regulations。Port Drug Administration shall be in accordance with the implementation time limit of electronic regulatory varieties stipulated by the State Food and Drug Administration,Corresponding to the implementation of electronic regulatory varieties during import filing review, check the product code according to its labeling production date,Those who do not give the code as required will not handle import filing,and notify the provincial food and drug supervision and management department where its electronic supervision agency is located。Portal Drug Administration corresponding to the variety of electronic supervision before December 31, 2013,Checking on January 1, 2014。Products produced after this date must be given according to regulations,Fang Fang can handle import stake sports betting appfiling; stake betting appthe non -code products that have been produced before this date should be completed by the import filing before April 30, 2014,Do not handle overdue。