OUR REGULATORY KNOWLEDGE
AT YOUR SERVICE
Our quality system, in compliance with reference source ISO 22716, checks and secures every step of the creation of your product. Traceability is provided by a batch file drawn up all along the process. Only a complete review of the batch file by the Quality Service allows the release of the product.
Our control laboratory, integrated to production workshops, makes physico-chemical, organoleptic and microbiological controls at different steps of the production:
Every commercialized cosmetic product has to be accompanied by a PIF (Product Information File) – identity card of the product – which must be at health authorities’ disposal throughout the product’s life. This file contains all data related to the product developed, such as qualitative and quantitative formula, the description of conditions of production and control, stability, innocuousness and efficiency tests results, safety evaluation, technical information about ingredients…
As part of the new regulation 1223/2009 becoming effective in 2013, M-LINE Laboratory commits itself to develop formulas in perfect harmony with demands of the new regulation and with specific regulations of various countries in which the products will be commercialized.
At your request, we draw up a cosmetic file in compliance with 2013 regulation. We guide you in all your regulatory procedures.
Challenge tests ISO 11930 standard
24 hours patch tests on 10 volunteers
Drawing up of the file preceding the confirmation
Confirmation of the toxicologist
Deposit at the CPNP (Cosmetic Products Notification Portal)
Specific tests according to properties of the product
Control of raw materials received and quarantining to make a physicochemical and organoleptic control
Control of unpacked products under production: pH, viscosity, density, microbiology and organoleptic quality
After each production, all the documents (production report and certificates of analysis of the finished product) are at your disposal.