PIM Group Regulatory Services
We are always by your side with our expert team for the domestic and international processes of registrations and regulatory affairs for your various products groups of especially cosmetics. You can get support from our company in all matters that come to your mind with respect to both legal processes and all other matters that you need. Please contact us for detailed information.
Cosmetic Company Registration
The companies that will be engaged in cosmetic activities for the first time should firstly required to register their company as a cosmetic manufacturer and/or importer. This registration must be made through both the Product Notification System (Ürün Takip Sistemi/ÜTS) and the Electronic Application System (Ürün Başvuru Sistemi/EBS).
Responsible Person for Turkey
According to the Turkey Cosmetic Law No. 5324, the manufacturer is a natural or legal person who produces, manufactures, corrects or introduces himself as a manufacturer by putting his name, trade mark or distinctive mark on the product; if the manufacturer is outside of Turkey, representatives authorized by the manufacturer or importer; is also a natural or legal person in the supply chain of the product or whose activities affect the safety aspects of the product.
Cosmetic EU Responsible Person
The Responsible Person is responsible for ensuring that all obligations related to legislative conformity of the product are fulfilled before entering to the European Market and acting as a point of cosmetovigilance contact in Europe for the cosmetic product for which it is responsible.
Cosmetic Products Notification Portal (UTS)
Pursuant the Cosmetic Law No: 5324 entitled, it is an obligation to notify the Ministry of Health before cosmetic products are made available on the market. In addition, the Cosmetic Law No: 5324 entitled Notification and Inspection, it is an obligation to notify the Ministry of Health before the cosmetic products are made available on the market for the first time and notifying the changes occurring in the product or manufacturer after the notification.
Medical Devices Registration
Medical devices: Refers to device definitions contained in articles of entitled “Definitions” Medical Devices Regulations published in the official newspaper dated 7/6/2011 and Active Implantable Medical Devices Regulations published in the official newspaper numbered 27957 and dated 7/6/2011.
Active substances and preparations containing one or more active ingredients, offered for sale ready to use, controlling over the target organism in terms of chemical or biological aspects or restricting the activity of such organisms and making it harmless or destroying are classed as biocidal products.
Food supplement in order to supplement a normal diet; products containing feed items such as vitamins, minerals, protein, carbohydrates, fiber, fatty acids, amino acids or nutrients in plant and animal origin ingredients, concentrated or extracts, and bioactive substances similar in the form of capsule, tablet, lozenge, a package of disposable dust, liquid, ampoule, dropper bottles alone or in mixtures and other similar products prepared in liquid or powder form administered at designated dose and daily intake.