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Quality Management


Our top goal is to satisfy our customers' requirements. Our efforts are directed at gaining and keeping customers' trust and confidence. We set high standards for our products and services and consistently satisfy them through strict adherence to our quality policy.

Medical device manufacturers in Europe are legally required to have a quality management system which complies with EG Directive 93/42/EEC Medical Devices Act and DIN EN ISO 13485 standards for Quality Management Systems. More stringent regulations and certifications that apply to worldwide trade have been integrated in the BEKA Hospitec QM system. Internal audits are conducted regularly in all operational areas and annual external audits are made by the Notified Body of the TÜV SÜD in Munich. This internationally respected technical services company (TÜV SÜD) has certified products and quality management systems for international markets for many years. These ensure us a high level of quality, particularly in processes in Research and Development, Supply Chain Management, Production, and Quality Management and also in our products and services.