Future Diagnostics has built a Quality Management System that meets the requirements of the international standards ISO 9001 and ISO 13485, as well as the Quality System Regulations of the FDA (CFR 820). Assays are produced in compliance with the European IVD Directive.
The Quality Management System of Future Diagnostics is a framework that ensures its commitment to meet customer’s expectations and regulatory requirements and to achieve the company’s quality objectives.
Each process within the organization of Future Diagnostics is monitored by internal and external audits and by measuring process indicators. In conjunction with efficient communication and decisive management, this guarantees a system of continuous improvement.
Our quality initiatives are further supported by an organization that brings broad experience, and up-to-date knowledge of new techniques, and exemplifies flexibility, transparency and efficiency. In addition, we are committed to meeting or exceeding the expectations of our clients, and we ensure that we accurately register their requirements before we start every project. Upon completion of a project, Future Diagnostics conducts an internal evaluation so that continuous improvements can be made.
You can download here our ISO 9001 and ISO 13485 certificate.