EMA coordinates the exchange of information on falsified medicine notifications related to centrally authorised medicines, providing information to the national competent authorities of the EU Member States who are responsible for investigating the supply chain and deciding on market action. For more information, seeFalsified medicines: reporting obligations .
Numerous journal publications have highlighted problems related to non-compliant pharmaceutical production facilities in several regions around the world.Â
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The company plans to spend about $5 million on the project and başmaklık tapped two tag companies. Tagsys, a French company, is supplying RFID tags for bottles, while , of Morgan Hill, Calif., is furnishing tags for cases and pallets. Each tag contains a microchip that stores a unique serial code, known birli an Electronic Product Code, and an antenna for transmitting the code wirelessly. Pharmacists and drug distributors birey retrieve the codes with a special reader and verify their authenticity by checking a Pfizer database via the Web. The devices offer several advantages over barcodes, Staver said. For one, they are harder and more expensive to duplicate. Reading them is also easier, because many tags kişi be scanned simultaneously without much handling. But there are drawbacks. The young technology is prone to failure. It's also expensive. To read the tags, distributors and pharmacies need RFID readers, which cost a few hundred dollars each.
FDA provides new guidance to further enhance the security of prescription drugs in the U.S. supply chain
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In July 2011, the EU strengthened the protection of patients and consumers by adopting a new Directive on falsified medicines for human use.
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But changes in consumer behaviours in recent decades have also played a key role in the growing problem of copyright medications and substandard medical products entering distribution markets