Across Systems Publishes White Paper for Medical Technology

On its website, Across Systems has published a topical white paper on the subject of effects of official regulation on medical technology documentation. The white paper summarizes the changes of the new Medical Devices Regulation and shows how companies can tune their workflows to future regulations.

Medical technology companies are positioned around the world and market their products internationally. At the same time, hardly any industry is faced with such extensive and restrictive regulations for the creation of product-related information and its translation. A new Medical Devices Regulation (MDR) of the EU, which is currently in the final approval process, explicitly requires multilingualism and comprehensibility of the documentation. "Especially in medical technology, regulations have a major impact on the multilingual documentation. Thus, it makes sense to look into the internal documentation and translation processes and identify optimization potential", explains Dr. Frank Reininghaus, who takes care of customers in the life science industry at Across Systems.

The Across white paper summarizes the changes and shows how businesses can tune their processes to future regulations. White paper on the subject of effects of official regulation on medical technology documentation.

White Paper for Medical Technology.

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