Regulatory affairs

The cosmetic formulation has no secret for you but its marketing is still unclear. This article will help you to understand. Indeed, to comply with the regulations and be able to put market cosmetics in Europe, you must develop a Product Information File (PIF). This document which gathers all the essential information guaranties the safety […]

In our field, quality is very important. This is why the internationally recognized ISO 13485 standard establishes the requirements for a quality management system specific to the medical device field. In 2016, this standard was reviewed to allow convergence towards European regulatory requirements and to better comply with the changes in the field of quality […]