Jul 30, 2018 Retrieved from https://www.recipharm.com/manufacturing/serialisation. Contact Us. Esco Pharma Pte. Ltd. 21 Changi South Street 1 Singapore
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).
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 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). 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 has equipped its sixth facility with serialisation capabilities ahead of the US and European regulation enforcement deadlines.
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 in Fontaine has extensive experience in manufacturing and packaging tablets and capsules using conventional granulation as well as state-of-the-art fluid bed granulation. The site will also house the Recipharm show-case line for serialisation, running from mid-2016, thus making it a centre of excellence for this technology. Jun 6, 2017 Erik Haeffler, vice president of manufacturing services, Recipharm, in the landscape of serialisation that contract partners must overcome.
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 facilities in Brescia, Italy and Karlskoga and Uppsala, Sweden, are the latest of Recipharm’s sites to be 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). RECIPHARM, the contract development and manufacturing organisation (CDMO), has formed a global partnership with Marchesini, SEA Vision and TraceLink to introduce new serialisation capabilities.
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.
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.
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
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.
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Recipharm serves more than 250 customers and expects 85% of its production to require serialisation. Recipharm launches serialisation showcase line. 7-Oct-2016 .
Status/uppdatering från parallellimport Serialization in European and Russian Markets.
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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 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. The complete serialisation solution will be implemented in 15 of Recipharm’s European locations and on more than 70 production lines.