LIDERMED, S.A. quality and certifications
Quality as the foundation of medical device manufacturing
LIDERMED, S.A. began its activity in 1986 as a manufacturer of healthcare products, with a constant commitment to innovation, continuous improvement and customer service. The quality policy defines the reference framework to ensure that processes, products and professional relationships are developed with rigour and responsibility.
Quality management system
The implementation and maintenance of the Quality Management System in accordance with UNE-EN ISO 9001:2015 and UNE-EN ISO 13485:2016 reinforces LIDERMED’s commitment to safety, traceability and consistency in medical devices. These standards are particularly relevant in an environment where documentation, process control and continuous improvement are essential.
Quality commitments
1. Comply with the legal, regulatory and contractual requirements applicable to the activity.
2. Apply continuous improvement to processes and products in order to optimise resources, reduce waste and improve final quality.
3. Maintain a close relationship with customers and interested parties to strengthen satisfaction and trust.
4. Communicate internally that quality affects every area of the company, from production to customer service.
5. Create a work environment based on commitment, teamwork, trust and mutual respect.
What quality provides to B2B customers
For hospitals, distributors, orthopaedic retailers, pharmacies, brands and OEM customers, quality is not only a documentation requirement. It is a factor of safety, supply continuity and professional trust. A robust management system facilitates supplier approvals, audits, documentation requests and more demanding purchasing processes.
Certificates
