As a medical device manufacturer, VIVACY is subject to regulations and standards governing products and quality management systems. This ensures continuous improvement is built into it’s processes and procedures. The company’s continuous improvement activities apply to all of its medical devices.
The quest for the highest quality begins with regular audits of suppliers, a rigorous selection of raw materials, the qualification of manufacturing process, control of work areas (ISO Class 7 Clean Room, ISO 5 flow), final analysis before release, and last but not least, the high level of staff training.
VIVACY fully controls every aspect of the production process to ensure that all gels are perfectly pure and homogenous. Specifically trained operators carefully and individually control each syringe before being packaged. All these safety measures and precautions are taken to provide a safe final product of high quality and high performance.
Driven by its growing success, VIVACY has built a new high-tech 3,500 square meter manufacturing facility in the Haute-Savoie region of France, 10 minutes from Geneva. The new factory has become a centre of advanced manufacturing technologies, innovation, research and product development in compliance with European and International standards and regulations.