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Quality management system for medical devices, the ISO 13 485 standard and the impact of the new RDM 2017/745 regulation
A quality management system applied to medical devices is governed according to ISO 13485. This non-mandatory standard applies to organizations involved in one or more stages of the life cycle of a medical device ranging from design to development and also including production, storage, distribution and post-market surveillance. Companies working...
Responsibility for Industrial IT Systems
Processus Projet (Agile, ITIL), devOps & DevSecOps method (Build, Run, Tests...)...
Development of a web application in the hospital sector
Patients, upon leaving the maternity ward, are cared for by midwives at home in order to extend their somatic and psychological monitoring....
Cloud migration and web portal creation
In the context of a takeover, our client needs to accelerate its technological evolution in order to make the transition to “Full Web”....
Will your business be affected by the RPA?
Among the best known, we find printing which (among other things) replaced manual copying and marked the disappearance of copyists, tractors which deprived draught horses of their last utilitarian role, driving them to the brink of extinction, and the digital camera which almost replaced the analogue camera and contributed to...
Artificial Intelligence – Detecting birds close to wind turbines
Avian mortality due to collision with wind turbine blades is very high. To reduce or even eliminate these accidents, rapid and accurate detection of the birds is necessary in order to take measures to scare them away or to stop the machines....
