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

The company has devised a pricing structure that will see the removal of any upfront investment costs for pharmaceutical companies looking to access the CDMO’s serialisation capabilities.Recipharm will offer a standard solution across 14 locations in Europe and more than 70 production lines, with a fixed service fee per pack for all customers.

Serialization involves placing a unique code on pharmaceuticals that allows them to be easily identified and tracked. The industry-wide serialisation, aggregation and verification directive is expected to improve traceability of drugs, help in the fight against counterfeit products entering the supply chain and ultimately improve patient safety. Recipharm serves more than 250 customers and expects 85% of its production to require serialisation. 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 The complete serialisation solution will be implemented in 15 of Recipharm’s European locations and on more than 70 production lines.

A Recipharm’s serialisation programme was recently recognised in the TRACKTS Awards 2017 as an example of best practice for its execution of a track and trace system at the Lisbon facility following a detailed assessment of the project’s methodology, use of technology and innovation. Contact information 2016-05-24 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 invites customers to a serialisation open day which will be held at our Brescia facility in Italy on Thursday 16th November 2017. This is a unique opportunity to increase your knowledge and understanding of the EU Falsified Medicines Directive (EUFMD) Safety Features Delegated Regulation.There will be presentations and a site tour with the chance to see a serialisation line in … Recipharm announces all its facilities are ready for EU serialisation Thu, Feb 14, 2019 10:00 CET. Recipharm, the contract development and manufacturing organisation (CDMO), today announced that all fifteen of its facilities outlined in its investment plan are now fully prepared for drug serialisation and have delivered serialised batches within Europe ahead of the February 9th deadline. 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.

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 …

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 .

Orebro, Sweden Project Manager and Production Engineer, Recipharm Pharmaceuticals Education Örebro universitet 2004 — 2007. Ingenjör för Projektledning

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 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. Recipharm’s three-year serialisation programme began in January 2016 and involves a 40-million-euro investment.

In 2018, Recipharm launched a standalone serialisation service, meaning we can take care of your serialisation requirements even if your products are not manufactured within Recipharm. At Recipharm, we offer: Serialisation and aggregation of secondary packaging, including blisters and bottles 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). 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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About Recipharm Recipharm announces all its facilities are ready for EU serialisation Thu, Feb 14, 2019 10:00 CET During the period 2016-2018, the CDMO invested EUR 35 million into its operations and launched a three-year programme to provide a compliant serialisation solution for its customers, ahead of the introduction of the EU Falsified Medicines Directive (EU FMD) and the US Drug Supply Chain Security Act (DSCSA). Moving forward Recipharm will be able to add 2D codes, human readable text and tamper evidence to pre-packed medicines using existing equipment across its facilities, they state in the press release. 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 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.

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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.

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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

2016-06-23 Recipharm’s serialisation programme was recently recognised in the TRACKTS Awards 2017 as an example of best practice for its execution of a track and trace system at the Lisbon facility following a detailed assessment of the project’s methodology, use of technology and innovation.

To meet the EU serialization deadline on 9 February 2019, pharmaceutical companies and their contractors have had to reorganize their manufacturing lines

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 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 announces global serialisation collaboration 23-Jun-2016 . Regulatory. The contract development and manufacturing organisation (CDMO) has formed a global partnership with Marchesini, SEA Vision and TraceLink to introduce new serialisation capabilities 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. Recipharm’s serialisation programme was recently recognised in the TRACKTS Awards 2017 as an example of best practice for its execution of a track and trace system at the Lisbon facility following a detailed assessment of the project’s methodology, use of technology and innovation. Contact information RECIPHARM, the contract development and manufacturing organisation (CDMO), has formed a global partnership with Marchesini, SEA Vision and TraceLink to introduce new serialisation capabilities. 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.