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.

Failing to recognise the scope of serialisation could lead to costly downtime and product shortages, as well as potential loss of business in key markets. In the Medicine Maker’s serialisation focused issue, Erik Haeffler, Vice President of Manufacturing Services at Recipharm outlines the complexities and challenges that serialisation brings for CMOs and the importance of getting ahead in

About Recipharm 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. 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. 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 serialisation

SPP Hållbarhetsrapport. RECIPHARM. Årsredovisning 2019. SPP FONDER Hållbarhetsrapport.

Dec 28, 2016 The DQSA mandates that all prescription drugs sold in the U.S. must be serialized at both the salable unit level and the case level by November

Serialisation is a means to trace and track pharmaceuticals from manufacture through to prescription, using bar codes to record information about product origin, shelf life and batch. This will help the fight against counterfeit products entering the supply chain and ultimately improve patient safety.

➱Complete L1-L5 solution, including hardware and software components. ➱ Built using a modular approach for different global mandates. ➱ Ensures the least

At Recipharm, we offer: Serialisation and aggregation of secondary packaging, including blisters and bottles; Ability to add 2D data matrices, human readable text Jul 13, 2020 Staffan Widengren, Recipharm, and Dexter Tjoa, Tjoapack, describe the The serialization of a product is a complex process that requires the PHARMA SERIALISATION EXPERTS. Serialization. Traceability. Secured.

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).
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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).

Erik Haeffler, VP of manufacturing services and head of CSR, shares Recipharm’s experience. We recognised the impact of the EU FMD quite early.
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Recipharm launches standalone serialisation service Mon, Jul 02, 2018 12:00 CET. 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). This month Erik Haeffler, Vice President of Manufacturing Services at Recipharm took to the Medicine Maker alongside other serialisation experts to discuss whether the industry is ready for the upcoming regulatory deadlines and to dispel the misconception that serialisation is simply ‘adding a label to the box.’. If companies can seize the opportunities that serialisation offers, then Recipharm equips a further three facilities for US serialisation Mon, Nov 27, 2017 09:00 CET. 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).

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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. The in

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 has equipped its sixth facility with serialisation capabilities ahead of 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.