Recipharm in Brescia on Vimeo vimeo.com/244990405

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 unveils serialisation pricing model Tue, May 24, 2016 09:00 CET. Contract development and manufacturing organisation (CDMO) Recipharm has unveiled plans to improve the affordability of serialisation, with the introduction of a novel pricing model aimed at keeping investment costs down for clients. 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). 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.

The new service is designed to offer pharmaceutical companies access to 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. Serialisation white paper Safeguarding the manufacture and delivery of our customers’ products is always a priority at Recipharm. 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 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. In February 2019, the new Falsified Medicines Directive (FMD) legislation for serialisation came into force, designed to guard against counterfeit medicines entering the supply chain. With no one-size-fits-all solution available for pharmaceutical companies to implement, many firms faced the challenge of altering legacy systems and processes in order to comply with the legislation before the 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.

As well as serialising over 500,000 packs for the US. Recipharm plans to establish another seven lines at the facility in the second quarter of 2018, according to a Monday statement.

Pharmaceutical Serialization: An Implementation Guide. By Joe Whyte, Global Serialization Lead, Rockwell Automation. Global pharmaceutical companies lose

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 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. The Lisbon […]

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.

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. The new service is designed to offer pharmaceutical companies access to Recipharm’s serialization capabilities as a standalone service due to increasing concerns that many will not be ready for the February 2019 compliance deadline, reports the company. 2D codes, human readable text and tamper evidence 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.
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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.

Stan Samuels ISPE.pdf The Korean project, which began in April 2014, required the Sweden-based CDMO (contract development and manufacturing organization) Recipharm to produce a data matrix code, including serial number, to comply with the regulations that are expected to be similar to what’s foreseen in serialisation in the EU. 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.
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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

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. 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.

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Martin Rasmussen ISPE Serialisation conference Lundbeck 20170921.pdf 7. Anders Vidstrup ISPE Presentation_2017-09-21_v2.pdf 8. Evren Ozkaya 20170921 SCW Digital Transformation Journey - Ozkaya v3.pdf 9. Staffan Widengren and Stefan Olofsson - Reser Recipharm Serialisation from a CDMO perspective September 2017 final.pdf 10. Stan Samuels ISPE.pdf

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.