As a globally active company, we are obligated to meet international quality standards as well as our customers’ many different organisational and medical needs. Naturally, the user interfaces and handbooks for VEPRO products are available in a wide variety of languages.
VEPRO guarantees the highest quality and stability for all products, with 100% data availability wherever possible.
The realisation, maintenance, and DEKRA monitoring of a quality management system in compliance with EN-ISO 9001 and EN-ISO 13485 guarantee that our customers have access to reliable products.
The VEPRO PACS / EMR is classified as a Class IIb medical product in Europe, which means that patient and device safety have the highest priority.
The FDA (510K) certification fulfils the requirements for using our PACS / EMR in the United States and many other countries.
VEPRO thus meets all national and international legal standards for medical products.