About Us
Tequir was founded in 1998 by a group of
companies distributing medical devices
mainly in spine, orthopaedics and traumatology technologies.
It was created with the purpose of providing a regulatory and importing service for complementary distributions that the members had, as well as an option for manufacturing its own medical devices.
In 2003, the company was certified in ISO 13485 and began to innovate medical devices by participating in several projects in collaboration with other teams.
In 2008, a corporate restructuring took place. Remeco S.A. and Maturana S.L., current shareholders of Tequir, decided to strengthen Tequir's capabilities in the field of medical device development, transferring the commercial part mainly to the company Keep Walking Project.
From that moment on, the company was renamed Tequir I+D+i. The aim of Tequir I+D+i is therefore focused on developing medical devices that provide improvements to current surgical techniques, mainly in the Musculoskeletal System. Tequir R&D&I, through its partners, is in direct contact with the market, which gives added value to the development team, which receives input to the design process based on the needs and problems detected by the clinical teams specialized in current medical technologies.
Over the years, Tequir has worked on a multitude of project involving medical devices of many categories and risk classification, which has given its team outstanding experience and expertise in healthcare regulation, medical device manufacturing technologies, healthcare management, clinical trials and post-market studies, process validation, planning, technical and economic feasibility studies and quality process performance.
SINCE 1998
Tequir’s team
CEO
Álvaro Alonso
Technical-regulatory direction
Magda Bresó
Administration
Nuria Dolz
PRODUCT DEVELOPMENT TECHNICIAN
Alejandro Hueso
PRODUCT SPECIALIST
Jose Miguel Manzano
QUALITY TECHNICIAN
Luis Marqués
PRODUCT DEVELOPMENT TECHNICIAN
Joan Garrigós
QUALITY TECHNICIAN
Blanca Esteban
SINCE 1998
Tequir certifications
EN ISO 13485
ISO 13485 is an internationally recognized standard for quality management systems in the medical device industry. It is intended and conceived for use in organizations for the design , development, production, installation, service and sales of medical devices. At Tequir we have had this standard since 2003.
