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Laetus and STADA partner for implementation of EU FMD

By February 2019, pharmaceutical companies in Europe must have implemented specified regulations.

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By: Greg Hrinya

Editor, Label & Narrow Web

By February 2019, pharmaceutical companies that manufacture or sell their products in Europe must have implemented the regulations specified in the EU Falsification Directive (FMD). This includes the traceability (Track and Trace) of prescription drugs back to the manufacturer.

STADA Arzneimittel AG responded to these requirements early on and initiated the appropriate measures. For the implementation of the serialization requirements according to EU-FMD, the manufacturer of generics and OTC brand products relies on Laetus GmbH as its partner. The project covers a total of 30 lines at the sites in Germany, Serbia, Montenegro, UK and Russia and involves a good deal of close collaboration.

In choosing Laetus, STADA Arzneimittel AG is placing its trust in a reliable partner with a proven ability to implement serialization projects of this scale and deliver success – backed up by more than 40 years‘ experience of inline quality control and hundreds of successful track and trace installations.

In addition to Secure Track & Trace software (S-TTS), Laetus also offers, among other things, some 20 MV-70-F pack handling systems with integrated weighing and manipulation protection functions (tamper-evident labelling). This machine is particularly suited to integration into existing packaging lines, thanks to its compact dimensions.

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