Certifications

The company will comply with the standard regulations ISO 13485:2003 during the prototype development and cell culture testing for medical diseases.

Safety in handle medical devices and testing them is a fundamental priority for our products, environment, lab and office space, and staff working in biomedical applications. Risk assessment is also taking in consideration.

ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.

QMD sensors will be full functional for the biomedical applications in few years , ISO 17851:2016.

Material durability forecast in relation to space environment impact is based on results of ground tests and mathematical modelling of processes of space environment effects on materials and on-board experiments. For high-precision forecasts, it is necessary

provide a general description of the methodology in selecting a set of space environment components and their characteristics during spacecraft material tests, and
— determine general principles and criteria for the tests.

— to choose correctly the set of space environment components which affect a spacecraft in various space regions, and to define their characteristics authentically,
— to select the principle and minor physical and chemical processes causing the material degradation under the space environment impact, including possible synergistic effects,
— to define the requirements to conditions of the ground-based material tests and to applied physical and mathematical models,
— to define the criteria for structural and functional material durability to the space environment impact, and
— to select the correct methods of material durability forecasting for different spacecraft lifetimes in various space region.