I tre år har Recipharm genomgått en rad av stora investeringar: 1) 3) förvärv av nya kunskaper: serialisation för att spåra droger (krav från och

That's why we are committed to meeting the latest pharmaceutical serialization and track & trace regulations designed to prevent falsified medicines.

He has Why serialization? Compliance: Changes in regulations by leading bodies such as US Food and Drug Administration (USFDA) and the European Medicines Mar 27, 2018 Expansion increases the facility's manufacturing capacity by 200 million unidoses /year. Recipharm's new blow-fill-seal machinery is now 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 Pharma Serialization is assigning a unique code to the packaging of each drug and printing this code on the packaging by any method. Pharmaceutical Serialization: An Implementation Guide. By Joe Whyte, Global Serialization Lead, Rockwell Automation.

Recipharm serialisation

Recipharm, the contract development and manufacturing organisation (CDMO), has launched a showcase line for serialisation, offering pharmaceutical companies the chance to view and trial its solution to the new European and US regulations. 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 , 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 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 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 contract development and manufacturing organisation (CDMO), has kick-started its campaign to introduce its customers to new processes for pharmaceutical serialisation 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. 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, a leading contract development and manufacturing organisation (CDMO) has equipped its sixth facility with serialisation capabilities ahead of the US and European regulation enforcement deadlines.

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. 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. 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. 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 launches serialisation showcase line. 7-Oct-2016 .

Get to know more about the specific requirements of your supply chain with a serialisation process that helps keep us at the forefront of the CDMO industry.
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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 Recipharm has already delivered over 1.3 million serialised and aggregated packs to markets such as China, South Korea, Saudi Arabia and Turkey, and 0.5 million packs to the US, where serialisation regulations are currently in place. 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 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 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’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 launched a showcase line for serialisation, offering pharmaceutical companies the 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 About serialisation 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.
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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.

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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 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, 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 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.

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. Holmes Chapel, England, United Kingdom57 connections. Join to Connect. Engineering Lead for Serialisation program. Recipharm. Dec 2015 - Mar 2018 2 years 4 months. Stockholm, Sweden.