High resolution printer REA JET HR for worldwide serialization tasks - REA JET HR

REA at the Achema: Final burst for the Pharma serialization

Muehltal, May 29th, 2018 – From February 2019, the anti-counterfeiting directive 2011/62/EU and the delegated regulation (EU)2016/161 will apply to pharmaceuticals. Packaging of prescription drugs must then have security features such as tamper evidence and a serial number. At the Achema show REA presents latest technology coding and marking systems as well as code verification systems that implement standard-compliant marking and ensure compliance with the required code quality.

REA's experts have extensive know-how on the global and national requirements for serialization. In addition to modern, high-resolution identification and code verification systems suitable for industry 4.0, REA also provides the necessary technical documentation (IQ, OQ, HDS, SDS etc.), which can be used to compile URS and SOPs if required. REA VERIFIER optical code verification systems meet the CFR 21 Part 11 requirements with regard to data storage and user administration and support a complete audit trail as well as user administration with multiple roles.

REA presents future-proof solutions for variable and effective primary, secondary and tertiary package marking with inkjet, laser and labels. The presented systems mark products with batch numbers, expiry dates, bar codes or data matrix codes, serial numbers and GTIN, thus enabling an end-to-end serialization and traceability. All hardware and software solutions from REA are "Made in Germany". The company also has numerous low-emission and solvent-free certified inks in its portfolio, particularly for the pharmaceutical and food industry.

For technical discussions and information exchange at the REA booth (hall 3.1, booth C48), professional experts will be available to discuss various topics from the field of pharma serialization.

Under the motto "Exchange of experience at REA" you can meet as follows:

Wednesday, 13.6.2018, 13:30 - 14:30 o´clock 
securPharm e.V.: Mr. Martin Bergen (Managing Director securPharm e.V.)
Topic: “Implementation of the Counterfeiting Directive - Countdown is on”

Hall 3.1 - Booth C48

+49 (0) 6154 - 638 0

You have questions? We would be pleased to call you back.

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