With people’s increasing attention on rationality and safety of drugs, subtle changes in drugs production and circulation will be a focus of public. By means of modern technology, information administration has become an important weapon for governmental authorities, manufacturing and distributing enterprises as well as public to jointly realize the full transparence of drugs administration.

Followed by the electronic administration on narcotic drugs, psychotropic drugs of category I and four categories of drugs with high risks, another 307 drugs that listed in Basic Medicine Catalogue will be added in drugs electronic administration network before March 31, 2011 to realize electronic administration in an all-round way. Otherwise, the drugs shall not involve in bidding and purchase process as basic drugs.

How to guarantee the “identification” of drugs--drug electronic supervision code to be successfully established? Drugs manufacturers shall observe the following three renovations to make the drugs with eligible drug electronic supervision code and the traceability:

First, code printing: to complete redesigning and code printing of packages or labels of all stages. New package suppliers shall be selected or require the original suppliers to add proper supervision code making equipment.

Second, production line renovation: select, install and debug the proper supervision code printing and relevant systems for packaging line. Drugs manufacturers shall select proper professional system integrators to complete data collection of drug administration code and establishment of relevant relationship in the production line.

Finally, renovation of finished products warehouse: establish in-stock data collecting system for finished products warehouse and record the supervision code data of out-stock drugs as well as the next receiver of the drugs. Similarly, drugs manufacturers shall select professional system integrators and equipment. In general, renovation of production line and finished production warehouse may be executed by the same experienced and professional system integrator.

Therefore, drugs manufacturers shall conduct intensive and complicated renovation in a few months. How to print the supervision code on package or label of relevant drugs? Which method or equipment can help the enterprises to print code at a lower cost? What kind of package supplier can help the enterprise to print the drug supervision code? What kind of system integrator can supply reliable and stable code printing production line and relevant system while ensuring the production efficiency? Which systems and equipment make the out-stock supervision code data collection more convenient and effective? All the questions will be answered in the 65th API China & INTERPHEX China “Drugs Electronic Administration Area”.

This exhibition actively responds to national policies and upon the request of drug manufacturers, the exhibition invites domestic and foreign outstanding code printing equipment manufacturers, packaging and printing enterprises as well as system integrators to exhibit the latest products and set up a platform for drugs enterprises and printing enterprises, printing equipment enterprises and system integrators so as to implement the national policies and seek concrete enforcement approach and solution for drugs manufacturers to obtain convenient electronic administration.

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Electronic Administration of Basic Drugs