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Dagens analyser - måndagen den 25 februari 2019 - Aktiellt

Recipharm, a leading contract development and manufacturing organisation (CDMO) has equipped three more of its facilities with serialisation capabilities in line with the US regulatory requirements in time for today’s introduction of the Drug Supply Chain Security Act (DSCSA). Recipharm, a leading contract development and manufacturing organisation (CDMO), has released its first serialised products to Europe from its facilities in Lisbon, Portugal and S Recipharm’s three-year serialisation programme began in January 2016 and involves a 40-million-euro investment. Staffan added: “This project milestone reaffirms Recipharm’s global leadership in serialisation and our commitment to meeting the compliance requirements well ahead of the February 2019 deadline. Recipharm, has received European Medicines Verification Organisation (EMVO) approval to submit serialisation data to the European Hub. The connection, which was facilitated by the company’ strategic partner TraceLink, is a milestone in Recipharm’s preparations for the Falsified Medicines Directive (FMD). Martin Rasmussen ISPE Serialisation conference Lundbeck 20170921.pdf 7. Anders Vidstrup ISPE Presentation_2017-09-21_v2.pdf 8.

Recipharm serialisation

To ensure that security is maintained from the production and packaging of medicines, to purchase by end consumers, we take responsibility for our link in the pharmaceutical supply chain with a serialisation process. Recipharm is a CDMO with serialisation firmly on our agenda. Download our ‘Serialisation - the facts’ brochure to find out how we help our customers on their journey to compliance. Recipharm launches standalone serialisation service. Recipharm, a leading contract development and manufacturing organisation (CDMO) has announced the launch of its standalone serialisation service ahead of the introduction of the EU Falsified Medicines Directive (FMD). The new service is designed to offer pharmaceutical companies access to Recipharm equips a further three facilities for US serialisation The facilities in Brescia, Italy and Karlskoga and Uppsala, Sweden, are the latest of Recipharm’s sites to be equipped to supply serialised products to the US and take the total number of facilities able to offer serialisation capabilities to nine. Staffan Widengren, director corporate projects at Recipharm, looks back on Recipharm’s approach to serialisation ahead of the FMD deadline and discusses the company’s future plans.

Kjell Johansson, President Manufacturing Services Europe, added: 'Those companies who fail to prepare for the new regulations will face major disruption to their product supply. As a leading Contract Development and Manufacturing Organisation, Stockholm-headquartered Recipharm has had to grapple with the demands of serialisation both in terms of its internal needs and those of its customers and their supply chains.

Dagens analyser - måndagen den 25 februari 2019 - Aktiellt

7-Oct-2016 . Packaging | Regulatory.

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Engineering Lead for Serialisation program. Recipharm. Dec 2015 - Mar 2018 2 years 4 months. Stockholm, Sweden. Central Engineering Lead for the With today's DSCSA deadline, CDMO Recipharm now has nine locations able to supply serialized products to the U.S. · Jim Butschli.

The Lisbon […] Recipharm, a leading contract development and manufacturing organisation (CDMO) has equipped its sixth facility with serialisation capabilities ahead of the The serialisation of licensed drug products will be a legal requirement for companies in the EU from early 2019.
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Recipharm equips a further three facilities for US serialisation Recipharm, a leading contract development and manufacturing organisation (CDMO) has equipped three more of its facilities with serialisation capabilities in line with the US regulatory requirements in time for today’s introduction of the Drug Supply Chain Security Act (DSCSA). Recipharm is a leading pharmaceutical contract development and manufacturing organisation (CDMO) headquartered in Stockholm with over 20 years’ experience.

Recipharm is a leading pharmaceutical contract development and manufacturing organisation (CDMO) headquartered in Stockholm with over 20 years’ experience. Recipharm, a leading contract development and manufacturing organisation (CDMO) has equipped its sixth facility with serialisation capabilities ahead of the US and European regulation enforcement deadlines. The complete serialisation solution will be implemented in 15 of Recipharm’s European locations and on more than 70 production lines.
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The announcement marks the next step in the global CDMO’s plans to invest €40m over the next three years to ensure state-of-the-art solutions for serialisation processes. Recipharm’s three-year serialisation programme began in January 2016 and involves a 40-million-euro investment. Staffan added: “This project milestone reaffirms Recipharm’s global leadership in serialisation and our commitment to meeting the compliance requirements well … Recipharm launches serialisation showcase line.

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Örebro University, Orebro, Sweden - European Graduates

The company anticipates that a pilot showcase line will be operational from July 2016 to allow customers to view and trial Recipharm’s standard solution for serialisation and aggregation. As a leading Contract Development and Manufacturing Organisation, Stockholm-headquartered Recipharm has had to grapple with the demands of serialisation both in terms of its internal needs and those of its customers and their supply chains. Erik Haeffler, VP of manufacturing services and head of CSR, shares Recipharm’s experience. Recipharm AB has outfitted yet another one of its sites with serialization capabilities, further solidifying the company's position as a provider of the increasingly important regulatory service. Situated in Lisbon, Portugal, the site is Recipharm's sixth to receive such capabilities and adds four packaging lines to the company's larger arsenal. Erik Haeffler, vice president of manufacturing services, Recipharm With growing concerns surrounding counterfeit medicines and the threat they pose to patient safety, the pharmaceutical industry is introducing varying serialisation mandates across the global market.