Description The deadline for the introduction of serialization for medical devices and in vitro diagnostic devices is approaching. However, their implementation raises certain questions and challenges for manufacturers, importers, and authorized distributors. We are pleased to invite you to an online training seminar to introduce you to...
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Learn how to protect your production efficiency Many players in the pharmaceutical industry have been feeling the pain of serialization solutions that are not their “cup of tea”. SoftGroup often hears from your peers about these struggles: overpromised and underdelivered capabilities, high rates of unexpected issues and...
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Learn everything you always wanted to know about printing technology, printers, and printing cartridges A problem with the supplementing equipment in pharmaceutical manufacturing can sometimes be the tip of the iceberg. With more than a year after the Falsified Medicines Directive came effective in Europe and many...
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In the last years, the serialization landscape has undergone an overall change, with a huge count of new regulations coming into force. It's not a secret that the implementation of the serialization processes impacted operations for many pharmaceutical companies around the world. There are still new...
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Parallel Importers under the EU FMD It’s been one year since the European Union adopted the Falsified Medicines Directive as a means of combatting counterfeiting in the pharmaceutical industry. What has changed after EU FMD for the Parallel Traders? In this webinar, SoftGroup's Track & Trace experts...
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