Innobiochips is at the forefront of innovation in in vitro diagnostics. Through close contact with academic labs and clinicians, and a passion for innovation, our team has developed a unique expertise in the development, production and commercialization of new diagnostic technologies. By combining deep expertise in biology and biochemistry with a commitment to pushing boundaries, Innobiochips is ready to deliver breakthrough solutions that enable more accurate diagnosis and more personalized patient care.
Design, industrialization & production
Innobiochips combines an excellent understanding of scientific advances in biology and chemistry with strong engineering skills in materials, electronics, automation and software development.
Innobiochips optimizes technological concepts and adapts them to industrial constraints: design, prototyping, assembly, sourcing, manufacturing process engineering, logistics management, small-scale production, transition to mass production, quality and compliance management.
This interdisciplinary expertise results in a highly diversified portfolio of innovative diagnostic tools in various application areas such as infectious diseases, chronic inflammation, transplantation and transfusion.
This dual expertise translates into a highly diversified portfolio of innovative diagnostic technologies, including multiplex assays, cell sorting, centrifugation, etc.
Quality Assurance
As an ISO 13485 certified company, Innobiochips guarantees the strictest compliance with international quality and safety standards for the design, manufacture, installation and maintenance of medical devices.
Applied to the innovative technologies it develops, Innobiochips offers a robust risk management system that facilitates access to international markets for its technologies.
Extended to all Innobiochips activities, the ISO 13485 standard enables our teams to continuously improve internal processes and optimize the use of resources.
Regulatory compliance
Regulatory compliance is essential to bring new IVD technologies to the market. Innobiochips developed a specific know-how to address the heavy regulation applied to IVD in Europe (IVDR): Premarket / Medical Device Reporting / Corrective and Preventive Actions / Postmarket Surveillance / Clinical Laboratory Improvement Amendments.
Our team offers an exhaustive know-how to meet regulatory goals in the EU, and maintain compliance throughout the whole product lifecycle.
Technology transfer
Innobiochips, a partner of major industrial groups in the life sciences sector, has developed extensive know-how in technology transfer and in adapting its technologies to industrial constraints. Innobiochips rapidly translates its technology design into a scalable and efficient manufacturing process, mobilizing state-of-the-art manufacturing techniques, automation, and quality control procedures.
Training and support
Innobiochips provides customized training and support programs to ensure smooth and rapid adoption of new diagnostic technologies in laboratories and healthcare centers.
A dedicated team manages troubleshooting for users and/or partners and is responsible for leading the change control process to ensure continuous improvement of commercialized products.