China's Best One-Stop Medical Equipment Provider
About

Company created in the year 1998 by a group of distributor companies in the field of spine, orthopedics and traumatology to serve as a regulatory base and import company of complementary distributions and to manufacturing in house products for the group of GAT companies. In the year 2008 a restructure takes place among the associates, and Remeco S.A. and Maturana S.L., the current shareholders of Tequir, decide to substancialy enhance the capacities of Tequir in the field of I+D, separating from Tequir everything related to import and distribution of medical products, actually managed by the company KeepWalking Project. The company is called Tequir I+D+I and its mision is to develop implantable medical devices that provide improvements to the current surgical techniques, principally in the musculosketetal system. Tequir I+D+i is in direct contact with the field and market, which results in an added value to the developing team. The set of development capabilities within Tequir, in combination with a constant update and actualization of the applicable technologies in the field of Medical Device Products, make Tequir I+D+i an ideal partner for the development of novel ideas, from its conceptual envisioning till its complete development. Tequir I+D+i is leader of a European project within the 7th Frame Program, called StimulAIS, where we act as Coordinator and Technical Direction of the Project. www.stimulais.com. Our mission is to endeavor the development of projects that offer a superior quality of life to the patient, actively promoting the collaboration between specialized clinical teams and transfer all that work and illusion to a concrete goal: Reach the market with a product that solves a problem.

Technologies
Outlook Microsoft Office 365 reCAPTCHA WordPress.org Apache Google Font API Mobile Friendly Google Tag Manager IoT AI
Keywords
anodized cleaning packaging & conditioning of medical devices in clean room assessment service for medical device product regulation clinical trial medical device product development medical equipment manufacturing regulatory strategy additive manufacturing in healthcare product design medical devices iso 13485 medical device validation clinical trials clinical research services clinical evaluation product registration ce marking medical device clinical validation product certification medical device and equipment manufacturing medical device regulation consulting regulatory documentation research and development in the physical engineering and life sciences regulatory affairs iso 10993
Company Information
  • Employees 8
  • Founded 1998
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