Recipharm equips a further three facilities for US serialisation. 27-Nov-2017 . Contract Manufacturing. Recipharm, a 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 the introduction of the Drug Supply Chain Security Act (DSCSA), 27 November 2017

Recipharm serves more than 250 customers and expects 85% of its production to require serialisation. 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.

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. 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). The complete serialisation solution will be implemented in 15 of Recipharm’s European locations and on more than 70 production lines. 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.

Recipharm 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). Staffan Widengren representing Recipharm AB in the ICSE theatre on Tuesday 4th October 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 equips a further three facilities for US serialisation.

The facility in Lisbon is the latest of Recipharm’s facilities to be prepared to start supplying serialised products to the US and Europe, following a EUR 40 million investment into its company-wide implementation programme in 2016. Recipharm, a leading contract development and manufacturing organisation (CDMO) has equipped its sixth facility with serialisation capabilities ahead of the US and European regula Recipharm, the Stockholm-based CDMO, has announced that all fifteen of its facilities are now fully prepared for drug serialisation under the new EU Falsified Medicines Directive (EU FMD). The company said it has already delivered serialised batches within Europe ahead of the 9 February deadline.

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.

Semcon has supplied three projects to pharmaceutical company Recipharm to which means that all prescription medications have to be serialised – or,

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. Recipharm, a leading contract development and manufacturing organisation (CDMO) has equipped its sixth facility with serialisation capabilities ahead of the US and European regula Recipharm equips a further three facilities for US serialisation Mon, Nov 27, 2017 09:00 CET 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. Recipharm launches serialisation showcase line. 7-Oct-2016 . Packaging | Regulatory. Recipharm’s new line is the latest step in a €40 million project to implement a state-of-the-art solution for its customers’ serialisation requirements across its 75 production lines in Europe Recipharm itself expects 85% of its own production to require serialisation, and therefore upcoming challenges are high on the CDMO’s agenda, driving serialisation investments of around €40m ($44m) over the next few years including direct technology investments with Marchesini, SEA Vision and TraceLink, announced last week.
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Staffan Widengren and Stefan Olofsson - Reser Recipharm Serialisation from a CDMO perspective September 2017 final.pdf 10. Stan Samuels ISPE.pdf Recipharm, a leading contract development and manufacturing organisation (CDMO) has equipped three more of its facilities with serialisation capabilities in line with the US regul The serialisation of licensed drug products will be a legal requirement for companies in the EU from early 2019. Swedish contract development and manufacturing organisation (CDMO) Recipharm plans to invest €40m over the next three years to ensure state-of-the-art solutions for serialisation processes.

Recipharm, the leading contract development and manufacturing organisation (CDMO), is pleased to announce its readiness for serialisation and the successful completion of a complex serialisation project for China on behalf of one of its customers. Erik Haeffler, VP of manufacturing services and head of CSR, shares Recipharm’s experience. We recognised the impact of the EU FMD quite early. Pre-studies started around 2013, and the project kicked off in 2014.
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Recipharm has equipped its sixth facility with serialisation capabilities before the US and European regulation enforcement deadlines. The facility in Lisbon is the latest of Recipharm’s facilities to be prepared to start supplying serialised products to the US and Europe, following a EUR 40 million investment into its company-wide implementation programme in 2016.

This is a unique opportunity to increase your knowledge and understanding of the EU Falsified Medicines Directive (EUFMD) Safety Features Delegated Regulation. Recipharm, the leading contract development and manufacturing organisation (CDMO), is pleased to announce further serialisation success with the completion of a complex serialisation project for Korea for one of its leading customers; Abbott.