The UNI EN ISO 22716 standard lays down the Guidelines for the production, control, storage and shipment of cosmetic products with the aim of guaranteeing the consumer high standards of safety and sanitation. These guidelines provide organizational and practical indications for the management of human, technical and administrative factors that influence the quality of cosmetic products. The standard constitutes the harmonized reference text to demonstrate compliance with Good Manufacturing Practice required by Reg. 1223/2009 (GMP), in force since 11 July 2013.
The ISO 13485 “Medical devices – Quality management systems” 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 and applicable regulatory requirements.
ISO 9001 is the reference standard for those who want to subject their production process to quality control in a cyclical way, starting from the definition of the requirements (expressed and not) of the customers, to the monitoring of the entire process / production process. The customer and his satisfaction are at the center of ISO 9001; every activity, application and monitoring of activities / processes are indeed aimed at determining the maximum satisfaction of the end user. The phases of application of the standard start from the definition of the procedures and registrations for each single process or macro process identified within the company organization.
Our production facilities comply with the Good Preparation Standards (GMP) and we are registered on the European Cosmetic Products Notification Portal (CPNP) for the notification and sale of cosmetic products. We also hold a certificate of free sale in non-EU countries.