The quality of our services is confirmed not only by hundreds of satisfied customers, but also by certificates: ISO 22716, ISO 13485 and IFS HPC, which results in our customers’ success.
In addition to ongoing monitoring of the production process, we carry out statistical quality control of products at the output stage, as well as raw materials and packaging at the input stage.
Procedures based on the highest standards of product safety and quality in accordance with ISO 13485, ISO 22716 and IFS HPC guarantee contract manufacturing of cosmetics in keeping with current European law, as well as safety of all products leaving our production line.
The implemented procedures are regularly inspected by the recognized TÜV Rheinland certification body, which is confirmed by the certificates we hold.
The EN ISO 22716:2012 standard describes the principles for cleanliness, hygiene and safety during the on-demand production of perfumes and cosmetics that we manufacture in our factory. Based on this standard, we have developed procedures to ensure product compliance with customer-approved specifications, full traceability and elimination of the risk of mixing produced batches. Our goal is contract production of top-quality cosmetics, while safeguarding repeatability in individual lots. Contract manufacturing of cosmetics or perfumes on demand in our company is completely safe and of high quality. Perfume and cosmetics products are fully traceable, which directly translates into the profits of our customers. The effectiveness of our procedures is confirmed by the certificate of the prestigious auditing company, TÜV Rheinland. The production of perfumes commissioned by companies and other products always meets the highest quality standards, which results in both customer and consumer satisfaction.
Medical devices that are introduced to the market must meet certain legal standards, thus guaranteeing the highest quality, safety for consumers and compliance with their expectations. The prestigious ISO 13485:2016 standard specifies in detail the requirements to be met by a quality management system in a company manufacturing medical devices to order. The high requirements of this standard relate, among others, to: carrying out design analysis at each stage of product development, risk management or keeping detailed documentation. The quality management system implemented in our company is based on the ISO 13485:2016 standard, which guarantees that medical devices made in our factory are safe for consumers and cater to their needs.
The International Featured Standard (IFS) is an organization that aims to raise consumer awareness by improving the transparency in the manufacture of products sold in retail. Therefore, in cooperation with representatives of the largest retail chains, standards have been developed to enable transparent production for the end customer. IFS HPC is a standard for Household and Personal Care products.
We implement procedures based on the requirements of this standard, which ensure the manufacture of safe products characterized by high quality and compliance with current legal requirements. Thanks to regular audits, the effectiveness of the procedures developed by us is confirmed by the certificate of the reputable certification body, TÜV Rheinland.