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

2016-05-24

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).

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 launches serialisation showcase line. 7-Oct-2016 . Packaging | Regulatory.

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 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.

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.

Staffan Widengren representing Recipharm AB in the ICSE theatre on Tuesday 4th October 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.

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

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.

Strategies to prepare for serialisation. As a result of increasing concerns over falsified medicines, reimbursement fraud and theft throughout the pharmaceutical Semcon har levererat tre projekt till läkemedelsföretaget Recipharm för att se till De har under lång tid arbetat med att serialisera läkemedel och var i behov av Rosie-Marie Holmlund. Director Quality Management Recipharm AB. Recipharm ABMitthögskolan,sundsvall. Stockholm, SverigeFler än 500 kontakter. Eva Hanö.
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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, a leading contract development and manufacturing organisation (CDMO) has equipped its sixth facility with serialisation capabilities ahead of the 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.

This is a unique opportunity to increase your knowledge and understanding of the EU Falsified Medicines Directive (EUFMD) Safety Features Delegated Regulation. 2016-06-23 · 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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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

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.

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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, 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. 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.’ 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. 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.