Corporate Policy

Vida S.r.l. was founded in 2012 as a distributor of medical devices and cosmetics, targeting the market of aesthetic medicine, cosmetic surgery and professional beauty. These markets are constantly evolving, for this reason, being able to interpret these changes and, above all, trying to offer its customers high quality, safe, high-performance and innovative cosmetics and medical devices represents a challenge that Vida S.r.l. has decided to undertake making quality and professionalism its strong points.

Vida S.r.l. it is a strong reality and ready for changes for this in 2016
the company has created ISO 5, ISO 7 and ISO 8 clean rooms at its headquarters located in Via G. Galilei 4 Crespina Lorenzana as production laboratories for the crucial transition from distributors to manufacturers of cosmetics and medical devices.

Innovation and continuous research for new solutions that guarantee safety and performance represent the major objectives of Vida S.r.l.. Vida S.r.l. constantly invests significant resources in research and development, with the aim of creating cosmetics and medical devices that can respond to the increasingly demanding demands of the market and guarantee high levels of quality, safety and performance. Vida S.r.l. produces and markets the Ksurgery brand which presents itself as an ideal and competent partner for both safety, performance and quality of cosmetics and medical devices.

All Ksurgery cosmetics and medical devices manufactured and/or distributed derive from accurate sector and market analyses, aimed at understanding customer needs and guaranteeing high levels of safety and performance and ensuring collaboration with institutes and companies known at European and global level. These partnerships guarantee cutting-edge cosmetics and medical devices in terms of safety, effectiveness and composition, thanks to the constant commitment to research and development aimed at the continuous improvement of the company and the medical devices manufactured and/or distributed.

In this context, the organization has chosen to adopt a Quality Management System according to the UNI EN ISO 13485:2016 and UNI EN ISO 22716:2008 standards as a tool for improving its performance, controlling processes, increasing customer satisfaction and ensuring compliance with requirements, including those of a legislative nature.

As confirmation of the commitment towards the customer and the desire to invest in quality, Vida S.r.l. achieved two important milestones in 2020, namely two CE markings for two class IIa and class III medical devices.
It is Furthermore, a new laboratory dedicated only to the production of sterile medical devices was set up in order to dedicate separate environments and resources for cosmetic and medical production.

• Differentiate yourself on the market for quality, safety, performance and image.
• Continuously satisfy customer needs through constant attention to formulation innovation.
• Achieve full staff satisfaction through the valorization of human resources.
• Maintain and continuously improve the Quality Management System by providing the resources and means necessary to ensure its effective functioning.
• Pursue satisfactory relationships with suppliers.

• Increase process efficiency through constant performance monitoring.
• Guarantee a high production standard.
• Being a flexible company attentive to market dynamics and innovations.
• Enhance human resources through the growth of their competence and improve the internal potential of the company through the involvement, motivation and awareness of all collaborators so that each of them behaves in the dual role of Customer and Supplier: either as Customer, in demanding the maximum level of quality from those who carry out the work upstream of his position; or as Supplier, in ensuring the maximum level of quality in the product of his work, proposing improvements and committing to carrying it out correctly in order to avoid remakes.
• Maintain a stimulating work environment that encourages teamwork.
• Manage company activities in compliance with UNI EN ISO 13485:2016 and UNI EN ISO 22716:2008 standards, seeking continuous improvement of all processes.
• Establish and keep updated a "strategic plan", in which the objectives to be achieved are defined.
• Maintain compliance with Directive 93/42/EEC for legacy devices and update the quality system and documentation to ensure compliance with the new requirements of the MDR 745/17 regulation regarding medical devices.

The Top Management of Vida S.r.l. assumes the responsibility of disseminating and supporting, with the most appropriate resources and means, this Quality Policy, clarifying and assigning specific responsibilities for its implementation to each collaborator.