The need for packaging line control as well as further collaboration among supply chain partners was emphasized during AIM Expo’s panel discussion, “Serialization in the Pharmaceutical Supply Chain: Lessons Learned and Remaining Challenges,” moderated by Bob Celeste, Director, Healthcare, GS1 US.
When it comes to implementing item-level serialization, most of the pharmaceutical supply chain seems to be waiting for FDA’s next move, or for California’s deadline for electronic pedigrees to get closer. Nonetheless, Purdue Pharma and Pfizer keep forging ahead. These two pharmaceutical manufacturers have been at the forefront of the pharmaceutical industry in piloting and adopting automatic identification technologies at the unit package level to combat counterfeiting and diversion.
The Healthcare Supply Chain Association (HSCA) and the Healthcare Industry Supply Chain Institute (HISCI) have released the results of an independent survey regarding industry adoption and integration of identification technologies used to track items in the healthcare supply chain. These include unique product identification and location codes such as Global Trade Item Numbers [GTINS] and Global Location Numbers [GLNs].
As we celebrate the end of 2011, we'd like to take time to point out the year's top articles on www.pmpnews.com. Following are the articles published this year that drew the most page views.
Hapa has acquired Gottscho Printing Systems in an effort to create a single source for inline, in-house printing solutions for the pharmaceutical, medical, personal care, food, and FMCG industries. Hapa provides late-stage printing customization technologies, while Gottscho provides flexographic technologies. Both are known for providing on-demand printing technologies.
ROC IT Solutions reports that a major pharmaceutical manufacturer has upgraded its implementation of ROC IT Solutions technology for track and trace in Turkey. The company's distribution center in Turkey first deployed ROC IT Solutions software in 2009 to meet the Turkish Ministry of Health (MoH) directive for item-level serialization and upgraded after its parent company began using a newer version of ROC IT solutions in the United States.
The Global Harmonization Task Force (GHTF) has released its proposal for a draft guidance on a Unique Device Identification (UDI) system that could be used around the world. The goal of the guidance is to provide a common global framework for identifying medical devices, which could facilitate recognizing recalled items and reporting specific devices involved in adverse events. Comments on the draft are welcomed through April 30.
In February 2011, the European Parliament adopted the “Falsified Medicines Directive.” The legislation is intended to protect EU citizens from falsified medicines, which are defined as products that “may contain ingredients in the wrong dosage or no active ingredients at all.” A distinction is made between “falsified medicines” and “counterfeit medicines,” which are defined as “medicines that do not comply with EU law on intellectual and industrial property rights, such as registered trademarks or patent rights.” According to a mem
We hear a lot these days about sunrise dates in the global GS1 System of product identification and related supply-chain standards. A sunrise date is a date in the future, agreed to and typically announced years in advance, at which point an industry or market sector is expected to be prepared to implement a specific technology.