OEM cosmetics processing is a trend

Cosmetics are ubiquitous on the streets, essential to the beauty of many women. With the development of the cosmetics market, celebrity endorsements and media promotion are prevalent, with billboards and subway advertisements largely dedicated to cosmetics, resulting in high customer satisfaction. OEM cosmetics processing technology and service quality are continuously improving, and the number of OEM cosmetics processing manufacturers is gradually increasing. OEM cosmetics processing is a trend, with many brands opting for this method.

Why choose OEM cosmetics processing?

OEM cosmetics processing refers to the authorization of a brand to entrust a cosmetics factory to carry out agency processing and manufacturing for its own brand. The brand only needs to provide the registered trademark, outer packaging and design, and business license. The technology and patent rights of new products are owned by the entrusting party, and the factory cannot use these brand-related items to sell to third parties. For authorized OEM cosmetics processing factories, the entrusting party only needs to submit the business license and the application for registered trademark registration.

What is the difference between OEM cosmetics processing and OEM?

What is the difference between OEM cosmetics processing and ODM? This mainly reflects whether the cosmetics manufacturer provides design services. OEM cosmetics processing refers to the cosmetics manufacturer only producing according to the requirements of the brand owner. ODM processing refers to the cosmetics manufacturer participating in the product design and planning. The difference between ODM and OEM in cosmetics processing. 1. OEM cosmetics processing. OEM, translated as Original Equipment Manufacturer. That is, the cosmetics manufacturer provides the production equipment and site required for cosmetics processing. Generally speaking, the brand has its own formula and product packaging, requiring cosmetics manufacturers to...

What are the benefits of choosing OEM cosmetics processing?

With economic development and improvement in people's living standards, more and more people are paying attention to the cosmetics market and joining the ranks of beauty and cosmetics. In the OEM cosmetics processing industry, the vast majority of cosmetics brands do not produce cosmetics themselves, but instead transfer the production module to professional OEM cosmetics processing factories. Why is this? Some cosmetics brands that want to own their own cosmetics factories need to invest a large amount of capital, including site rent, factory construction, equipment purchase, and qualification certification. According to a rough estimate, this one-time capital investment requires at least tens of millions of yuan. Choosing a professional

Good news! Yangsen Pharmaceutical has been selected for the official honorary title of "High-tech Enterprise"

According to the relevant provisions of the "Management Measures for the Identification of High-tech Enterprises" and the "Management Work Guidelines for the Identification of High-tech Enterprises", the Guangdong Provincial Department of Science and Technology has identified Guangzhou Yangsen Pharmaceutical Co., Ltd. as a 2021 high-tech enterprise based on its comprehensive strength in technological innovation, enterprise growth, and economic contribution. The official list of the second batch of high-tech enterprises in Guangdong Province in 2021 has been officially announced, and Guangzhou Yangsen Pharmaceutical Co., Ltd. is honored to be selected and awarded the honorary title of "High-tech Enterprise" by the Guangdong Provincial Department of Science and Technology. Yangsen Pharmaceutical promises that the information submitted is true, accurate, complete, and free of false materials, misleading statements, or significant omissions. Guangzhou Yangsen Pharmaceutical Co., Ltd. (GuangZhou YangSen Pharmaceutical Co., Ltd.) owns an advanced independent R&D innovation center. It is a well-known high-tech enterprise specializing in the research, development, manufacturing, sales, and service of functional products. The company is located in the Yangsen Industrial Park in the beautiful Baiyun Lake area. With technology as its core, the company currently has 2 authorized invention patents, 10 invention patents under review, 3 utility model patents, 3 authorized copyrights, and 7 design patents. The group and its legal person own more than 500 trademarks. Many more formula patents are being applied for. Yangsen Pharmaceutical has passed the dual certifications of US GMPC and EU ISO22716.

Good news: Congratulations to our company on successfully passing the city health and health commission factory inspection

Yang Sen, relentless in R&D innovation

Good news: Yangsen Pharmaceutical has been successfully selected for the list of "Technology-based Small and Medium-sized Enterprises" by the Guangdong Provincial Department of Science and Technology. This is another official honor for Yangsen Pharmaceutical in its journey of independent research and development innovation and continuous development, and it is the Guangdong Provincial Department of Science and Technology's recognition of Yangsen Pharmaceutical's research and development and innovation capabilities. Guangdong Province's 6th batch of technology-based small and medium-sized enterprises in 2021 In the process of identifying "technology-based small and medium-sized enterprises", the Guangdong Provincial Department of Science and Technology conducted a comprehensive audit of Yangsen's business conditions, R&D personnel, R&D investment, R&D results transformation, independent intellectual property rights, and Yangsen R&D Innovation Center. On August 6, 2021, Yangsen Pharmaceutical was officially included in the list of "Technology-based Small and Medium-sized Enterprises" of the Guangdong Provincial Department of Science and Technology, marking the official affirmation of Yangsen Pharmaceutical's core independent intellectual property rights and its independent innovation and technological research and development capabilities. Yangsen, R&D innovation never stops!

Regulations on the Supervision and Administration of the Production and Operation of Cosmetics

Order No. 46 of the State Administration for Market Regulation The Measures for the Supervision and Administration of the Production and Operation of Cosmetics, which was adopted at the 12th executive meeting of the State Administration for Market Regulation on July 26, 2021, is hereby promulgated and shall come into force on January 1, 2022.

Frequently Asked Questions on Cosmetic Filing and Registration from the National Medical Products Administration

#Q1 How to obtain a user account on the Cosmetics Registration and Filing Information Service Platform? Answer: According to the "Regulations on the Management of Cosmetics Registration and Filing Information", domestic registrants, filers, domestic responsible persons, and cosmetics manufacturers must obtain a cosmetics registration and filing user account through the registration and filing information service platform before they can handle cosmetics registration and filing. Overseas registrants and filers conduct cosmetics registration and filing-related business through the user account of their domestic responsible person. Article 18 of the "Cosmetics Supervision and Administration Regulations" has the same requirements for cosmetics registrants and filers. Enterprises or other organizations that meet the requirements submit relevant materials to open registrant and filer accounts simultaneously, and can then carry out cosmetics registration and filing-related work without needing to open registrant and filer permissions separately. #Q2 Which cosmetics registrants and filers need to designate a domestic responsible person? Answer: Cosmetics registrants and filers located overseas must designate a domestic responsible person in China to handle cosmetics registration and filing, assist in conducting adverse reaction monitoring, and implement product recalls. If an overseas registrant or filer entrusts a domestic cosmetics manufacturer to produce cosmetics, the cosmetics are considered domestic cosmetics, but because the registrant and filer are overseas, a domestic responsible person needs to be designated; if a domestic registrant or filer entrusts an overseas cosmetics manufacturer to produce cosmetics, the cosmetics are considered imported cosmetics, but because the registrant and filer are domestic, a domestic responsible person does not need to be designated. #Q3 What are the differences between the domestic responsible person and the original on-site filing responsible unit? Answer: Compared with the on-site filing responsible unit stipulated in the original "Cosmetics Hygiene Supervision and Administration Regulations" and related regulations, the domestic responsible person not only needs to handle registration and filing on behalf of the registrant and filer, but also needs to fulfill obligations such as assisting in adverse reaction monitoring, implementing product recalls, and assuming corresponding quality and safety responsibilities according to the agreement. On-site filing responsible units that do not have the ability to fulfill the corresponding obligations of a domestic responsible person cannot act as a domestic responsible person to conduct cosmetics registration and filing. #Q4 What content should the domestic responsible person's authorization letter specify? Answer: The content of the domestic responsible person's authorization letter should at least include the following content and information: the names of the registrant, filer, and domestic responsible person, the authorization and authorized relationship, the scope of authorization, and the authorization period. If the authorization period is not clear, it is considered permanent authorization; regardless of whether the authorization letter includes assisting in conducting cosmetics adverse reaction monitoring, implementing product recalls, and cooperating with supervision and inspection, the domestic responsible person should fulfill the obligations of assisting in conducting adverse reaction monitoring, implementing product recalls, and cooperating with supervision and inspection according to the regulations. #Q5 Can the original authorization letter be used for the domestic responsible person? Answer: The original authorization letter for the on-site filing responsible unit for imported special-use cosmetics cannot be used. The original authorization letter for the domestic responsible person for imported general cosmetics can continue to be used (only for handling the import filing of general cosmetics). If the original domestic responsible person's authorization letter has been submitted to the accepting department and the original cannot be provided again, the domestic responsible person should upload a scanned copy of the original authorization letter through the registration and filing information service platform when opening the domestic responsible person's user account, and can submit a photocopy of the authorization letter when submitting paper documents. If an overseas registrant or filer intends to expand the scope of authorization handled by the original domestic responsible person, a new authorization letter must be issued. The domestic responsible person can first handle the cosmetics registration and filing user account by uploading a scanned copy of the new authorization letter through the registration and filing information service platform, and should supplement the submission of the original authorization letter and its notarized documents by September 30, 2021. #Q6 How to register and file cosmetics that use new raw materials in the safety monitoring period? Answer: After a new cosmetic raw material is registered and filed, the National Medical Products Administration will publicly announce the relevant information on the registration and filing management of new raw materials. Other cosmetics registrants and filers who use new raw materials to produce cosmetics should fill in the registration and filing number of the new raw materials when handling the registration and filing of cosmetics, and obtain confirmation from the registrant and filer of the new raw materials through the registration and filing information service platform before submitting the registration application and filing materials. Cosmetics registrants and filers who use new raw materials in the safety monitoring period to produce cosmetics should fulfill the obligations of using and monitoring the safety of new raw materials as stipulated in the "Cosmetics Registration and Filing Management Measures". #Q6 How to register and file cosmetics that use new raw materials in the safety monitoring period? Answer: After a new cosmetic raw material is registered and filed, the National Medical Products Administration will publicly announce the relevant information on the registration and filing management of new raw materials. Other cosmetics registrants and filers who use new raw materials to produce cosmetics should fill in the registration and filing number of the new raw materials when handling the registration and filing of cosmetics, and obtain confirmation from the registrant and filer of the new raw materials through the registration and filing information service platform before submitting the registration application and filing materials. Cosmetics registrants and filers who use new raw materials in the safety monitoring period to produce cosmetics should fulfill the obligations of using and monitoring the safety of new raw materials as stipulated in the "Cosmetics Registration and Filing Management Measures". #Q8 How to handle the registration and filing of cosmetics with entrusted production? Answer: For cosmetics registrants and filers who entrust the production of domestic cosmetics, the cosmetics registrants and filers or the domestic responsible person should obtain confirmation of the entrusted production relationship from the cosmetics manufacturer through the registration and filing information service platform before submitting the registration application and filing; for cosmetics registrants and filers who entrust the production of imported cosmetics, the cosmetics registrants and filers or the domestic responsible person should submit materials proving the entrusted production relationship when applying for registration and filing. #Q9 How to register and file cosmetics that must be used with instruments or tools? Answer: Except for brushes, cushions, and hairdressing tools that only assist in application, the safety assessment of cosmetics that must be used with instruments or tools should assess the safety under the conditions of use with instruments or tools. In principle, the accompanying instruments or tools should not have cosmetic functions, should not participate in the re-production process of cosmetics, and cannot change the way and mechanism of action of cosmetics on the skin. #Q10 Is it allowed to change the formula? Answer: The formula of registered and filed cosmetics is not allowed to be changed. According to the "Cosmetics Registration and Filing Management Measures" and the "Regulations on the Management of Cosmetics Registration and Filing Information", for registered and filed cosmetics, if the raw materials used change suppliers, resulting in unavoidable minor changes to the product formula, such minor formula changes are allowed, but the obligations stipulated in the "Measures" and "Regulations" should be fulfilled. Product formula changes other than this situation constitute new products and should be re-applied for registration and filing. #Q11 How to handle changes in the management department for general cosmetics filing? Answer: If the address of the filer or domestic responsible person for general cosmetics changes across provinces, resulting in a change in the filing management department, the filing number and filing supervision responsibility of the general cosmetics will also change, so re-filing is required. The original filing materials can still be used for re-filing, and the registration and filing information service platform will also set up corresponding functions to facilitate the filer and domestic responsible person to re-file.

Yangsen Pharmaceutical commissioned a professional research institute to conduct multiple tests on the workshop

Today, Yangsen Pharmaceutical entrusted Guangzhou Institute of Microbiology to conduct multiple tests on the workshop: Floating bacteria Sedimentary bacteria Suspended particles Mixed illuminance Temperature, humidity, pressure difference Total number of bacterial colonies in the air Attachment: 39. Production workshops should be divided into clean areas, semi-clean areas, and general areas according to the environmental control requirements of the product process. Develop a workshop environmental monitoring plan and conduct regular monitoring. (1) Check whether the clean area, semi-clean area, and general area are reasonably divided according to the product process; (2) Check the environmental monitoring plan and whether it is implemented according to the plan; (3) Check whether there are valid test reports. 1. Floor plan of workshop area division (three-area division), the floor plan should be able to identify the corresponding areas (can be integrated with the "production workshop floor plan" in item 36. 2. Workshop environmental monitoring system and corresponding environmental monitoring plan, monitoring records, and corresponding analysis, improvement measures report or record for unqualified situations. 3. Workshop bacterial count test report within one year: This report must be issued by a testing institution authorized by relevant national departments, or a self-inspection report from an enterprise with self-inspection capabilities and CNAS accreditation, or a self-inspection report issued by an enterprise using testing instruments and equipment that have undergone legal metrological verification and using legal standards. 40. The filling room and clean container storage room for the production of eye care, baby, and children's skin care cosmetics should meet the requirements of Class 300,000 cleanliness. Production areas should maintain the corresponding pressure difference according to the process quality assurance requirements, and the clean area should maintain a certain positive pressure difference with other production areas. Temperature and relative humidity control in the production workshop should meet the product process requirements. (1) Check the air detection report of the production workshop, refer to the Class 300,000 standard of "GB 50457-2008 Design Code for Clean Rooms in Pharmaceutical Industry"; check whether pressure difference indicating devices are installed in the production area; (2) Maintain a certain positive pressure difference between the clean area and other production areas; (3) Maintain a certain negative pressure difference between functional rooms that easily generate dust and other functional rooms. (4) Check the control requirements and monitoring system for temperature and humidity; (5) Check the implementation of the monitoring system. 1. Completion acceptance documents for the air purification system. 2. Class 300,000 air cleanliness test report within one year (test items should include at least suspended particles, floating bacteria/sedimentary bacteria, temperature, humidity, pressure difference, etc.), this report must be issued by a testing institution authorized by relevant national departments, or a self-inspection report from an enterprise with self-inspection capabilities and CNAS accreditation, or a self-inspection report issued by an enterprise using testing instruments and equipment that have undergone legal metrological verification and using legal standards. 3. Documents or relevant supporting materials for pressure difference, temperature, and relative humidity monitoring. 4. Monitoring records of pressure difference, temperature, and relative humidity.