Cosmet Group; It offers the fastest and most economical solutions for the preparation of written quality management documentation such as procedures and instructions, which are important for the creation and strengthening of your company's corporate identity, and for the realization of certifications in accordance with the company structure.
The International Accreditation Service: IAS and International Accreditation Forum - IAF accredited ISO 9001-ISO 22716-ISO 45001-ISO 14001-ISO 22000 Management System Certificates, Halal Certificate and CE Declaration, which you can use on your company's website, on your product labels, valid in all countries that will professionalize your corporate structure We would like to work with you for their documentation.
ISO 9001:2015 Quality Management System
ISO (International Organization for Standardization); It is the process of establishing and applying certain rules with the assistance and cooperation of all interested parties in order to obtain economic benefits in relation to a particular activity. Standardization is actually an activity that emerges as a result of the society's search for quality and affordability.
The main purpose of ISO is;
To facilitate the international exchange of goods and services.
To develop standardization in the world to ensure mutual agreements in scientific, technical and economic fields.
To harmonize, unify and make recommendations to national standards.
To establish international standards with the approval of all members.
To support the development of new standards that are suitable for national and international use.
To provide information exchange on the work of national and technical committees.
To cooperate with other international organizations related to standardization, to carry out standardization studies that will facilitate the work of these organizations.
Use and Benefits of ISO 9001 Certificate
ISO 9001 certification is requested by many customers. This document alone will provide a market advantage. However, this benefit is short-term. Apart from the market advantage, ISO 9001 provides organizations with a continuous improvement mechanism and discipline. However, obtaining the certificate does not mean that perfection has been achieved. In an ISO 9001 certified organization, every problem is seen as an opportunity for improvement. The most important thing to solve the problem is to ensure that it does not happen again. The results of the research conducted in 720 certified companies in Turkey reveal the benefits of ISO 9001 as summarized below.
Strengthening the image of the organization,
Better supplier relationships
Positive cultural change
Formation of quality awareness
Standardization and consistency
Increased efficiency and productivity
ISO 22716 Good Manufacturing Practices (GMP – Good Manufacturing Practices)
It is a series of protective measures prepared for the production of products such as food, medicine, cosmetics, medical devices that directly affect human health, in reliable conditions and systems, and prepared to prevent the possibility of infection (contamination) at every stage from the preparation of the product to its distribution and to increase reliability. In accordance with the Cosmetics Regulation adopted by it, all member and candidate countries are obliged to comply with good manufacturing practices in cosmetics for cosmetic production sites. Within the framework of the application started in Turkey, GMP Certificate will be sought both for the products to be sold in our country and for export.
ISO 22000 Food Safety Management System / HACCP- Hazard Analysis and Critical Control Point (Hazard Analysis and Critical Control Points Certificate)
It has been published as a food safety standard developed after many years of work by the ISO committee, which convened to identify and meet the increasing international needs for food safety.
It is based on the determination of the hygiene conditions (personnel hygiene, equipment hygiene, raw material hygiene, environment hygiene, etc.) required for healthy food production in food establishments and providing these conditions, determining the reasons that may pose a health risk for the consumer during the production and service phase and eliminating these reasons. It is a product reliability system. The system is a systematic approach that ensures that hazards affecting product safety are predetermined and controlled.
ISO 14001:2015 Environmental Management System
ISO 14001 Environmental management standard; It is one of the risk-oriented management standards that determines what will be done as a result of controlling the environmental effects of enterprises, identifying and evaluating possible environmental risks. First of all, environmental risks are determined, and then the measures related to these risks are placed on the standard infrastructure with a planning structure. The relations of institutions and organizations with the environment are defined and managed within this standard.
ISO 45001 Occupational Health and Safety Management System
It is an occupational and worker safety management system developed by the British BSI (British Standards Institution) and separated from ISO in this respect. The occupational safety standard that ISO is still developing to publish is ISO 45001.
ISO 27001 Information Security Management System
It is the ISO standard prepared and published for the storage, distribution and protection of all commercial and non-commercial information in institutions and organizations. It is among the popular standards developed by ISO.
ISO 10002 Customer Satisfaction Management System
It is an ISO standard produced in order to control and evaluate all relations of institutions and organizations with their customers and to fulfill their requirements and ensure their measurability. This standard, which was previously handled at the procedural level in ISO 9001, is a customer satisfaction management system that has been developed and has been approved for independent publication due to its increasing importance. It is also called customer complaint management.
It is a type of document given to products prepared in accordance with the conditions of Islam.
The product and the company that will receive the halal certificate should have;
- All processes of the product, starting from the raw material to the finished product stage, and all substances and additives in the product composition comply with Islamic criteria and humanitarian requirements in terms of origin, supply method and ways, and source of supply,
– All raw materials and/or processed, semi-processed etc. used in the product composition and in the post-production stages. The person, institution, organization, company, etc., from which the substances are supplied, should not have a situation that clearly contradicts the Islamic belief and life,
– The packaging materials and storage conditions of the product comply with humanitarian requirements and Islamic criteria,
- To have the qualifications in accordance with Islamic criteria, humanitarian requirements, health and cleaning conditions, nutritional requirements, both in the production stages of the product, in all the elements in the product composition, and in the effects that may occur with the combination of each element in the product composition,
– It is required that the producer does not have a clear violation of Islam with his belief and life.
– The producer fulfills its financial obligations in terms of Islam.
CE Certificate (Declaration)
CE Symbol The products within the scope of the New Approach Directives prepared within the scope of the New Approach Policy adopted by the European Union (EU) in 1985 to make the legislation regarding the technical structures of the products simpler and general in order to ensure the free movement of goods within the framework of technical legislation harmonization, It is a Union mark consisting of the initials of the words Conformité Européenne, which indicates that it has passed all necessary conformity assessment activities and complies with the requirements of health, safety and consumer and environmental protection.
The CE Certification process consists of the preparation of the technical file, the writing of the test report and the completion of the declaration. You can use the CE Symbol on the product label and export without any problems.
ISO 13485 Medical Device Quality Management System
ISO 13485 is a quality management standard that can be applied to medical device manufacturers with the title of requirements for regulatory purposes, published by the ISO institution.