Uzbekistan
Service Provider
Central Asia Group (CAG) is distinguished as a consulting firm in that it provides platforms for countries and governments to expand their businesses and industries worldwide. With its success in opening opportunities for Malaysian companies to explore and expand their opportunities in Central Southeast Asia, especially Tajikistan, CAG has set in motion a worldwide trajectory for cooperation in business, between and within countries and governments. Scope of Experiences and Vision CAG facilitates and connects (G2G) countries and companies by: Creating and building bridges between countries for G2G business, bilateral relations, cultural exchange, economic benefits and more. Acting as a liaison between countries to assist them in understanding each other as well as the facilitating effective business, communications and administration. Countries always have different cultures and protocols. This serves to bring them closer together and achieve the same goals including the vision for the country itself. CAG has the knowledge and know-how to successfully connect, engage and solve/resolve issues for delicate and multileveled projects. The firm puts projects and resources together, not for just governments, but also for international entities and individual clients. Clients include: governments, publicly listed companies, private companies, and individuals.
China
Mini size design, body fit, Waterproof IP67, Accurate algorithm support heart rate, blood pressure, blood oxygen, moving target, also support incoming telegram, alarm clock, USB charging, Camera control
Request for a quoteBelgium
A thorough toxicological evaluation on raw materials is key if your company has ambition to sell raw materials to European manufacturers, as the raw materials must meet certain requirements to guarantee their safe use in cosmetic products. By making this evaluation available, you increase the sales possibilities all over Europe. This is also a key step to be able to approach the big players (L’Oréal, Estée Lauder, etc.) who will consider you as a serious partners as you will show a non-negotiable approach to quality and ensure the highest level of effectiveness and safety to end-customers. Taobé’s safety assessors will be able to develop a Dossier including: -A full toxicological assessment report of the raw material, according to the SCCS Notes of Guidance, demonstrating the safety of the cosmetic ingredient/s according to the utmost authority in Europe. -A CLP SDS, to provide to importers for REACH notification.
Request for a quoteBelgium
The very first step of every cosmetics registration in Europe starts with the full assessment of the formula of the product to confirm it meets the EU requirements. During this step, our Safety Assessors will: - Check all documents related to the ingredient (MSDS/COA/Non-animal testing/IFRA, etc.). - Verify that the ingredients do not have restrictions established by European regulations and that the limits of use (if there are any) are in compliance. - Check that the ingredients used are suitable for cosmetics (cosmetic grade ingredients). - Check the toxicological profile of each ingredient. - Verify if the ingredient contains any impurity. - Check the SCCS opinions, industry guidelines and other regulations (REACH, CLP). - Calculate the MoS (Margin of Safety) for each ingredient and/or search for supporting documents (reliable literature) that declare each ingredient safe at the added dose in the finished product.
Request for a quoteBelgium
The CPSR consists of two parts, A and B: in Annex I of the Cosmetics Regulation, all the information that must be collected and processed by the Safety Evaluator in order to identify and quantify the dangers that the cosmetic product may present for the human health, namely: PART A contains information on the safety of the cosmetic product, such as: 1. Quantitative and qualitative composition of cosmetic products; 2. Physical/chemical characteristics and stability of the cosmetic product; 3. Microbiological quality; 4. Impurities, traces, information on packaging material; 5. Normal and reasonably foreseeable use; 6. Exposure to the cosmetic product; 7. Exposure to substances and calculation of the MoS; 8. Toxicological profile of substances; 9. Undesirable effects and serious undesirable effects; 10. Information about the cosmetic product. PART B holds the conclusion, the warnings and instructions of use to label, the scientific reasoning and the assessor's diploma.
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