The 8th Cosmetics Summit and the sharing of experience in applying for new raw materials on Zoop have been successfully concluded
On May 22nd, the grand opening of the 8th Yuncheng Tianyu Conference·Cosmetics Summit took place. In the morning session, pharmaceutical regulatory experts provided attendees with in-depth interpretations of common cosmetic filing issues and new regulations on ingredient supervision, empowering enterprises to accurately grasp industry trends.
In the afternoon session's "Innovation and R&D of New Cosmetic Ingredients" sub-forum, Luo Qinghuan, Compliance Director of ZOOP, delivered a high-value presentation titled "Requirements, Experiences and Case Studies for New Cosmetic Ingredient Registration". Drawing upon numerous typical cases from ZOOP's successful new ingredient filings, Ms. Luo provided attendees with practical insights.
With comprehensive case studies from ZOOP's extensive operational experience, Ms. Luo thoroughly explained the rationality requirements for naming new ingredients, along with key documentation points regarding production processes, functional evidence, and ingredient sourcing. This guidance helps enterprises avoid common pitfalls and improve approval rates during the new ingredient registration process.
As the supporting organization of the conference, ZOOP emerged as one of the most popular exhibitors through its professional, innovative and interactive approach. The booth not only featured engaging games and exquisite gifts, but more importantly attracted numerous attendees with its solid technical expertise and extensive compliance experience.
The ZOOP team provided tailored one-on-one consultation services to address enterprises' specific needs, offering customized solutions that charted a clear course for cosmetic companies' compliance development. With their down-to-earth professionalism and case-based guidance, the experts became a major highlight of the exhibition area, helping industry players navigate regulatory challenges while seizing new opportunities.
The services provided by ZOOP
As a professional compliance service provider, ZOOP has extensive expertise in new cosmetic ingredient registration and filing. Leveraging multiple successful cases, we have developed efficient and reliable submission strategies to offer the following services:
Guidance on Safety Monitoring & Evaluation Systems
Assist new ingredient registrants/filers in establishing robust safety risk monitoring and assessment mechanisms.
New Ingredient Research Report Preparation
Support clients in compiling comprehensive R&D reports based on provided ingredient information, development background, and latest research progress.
Preparation of Manufacturing Process Documentation
Advise applicants in drafting detailed preparation methods and production processes for new ingredients.
Quality Control Standard Development
Guide the formulation of quality standards, including:
• Stability test data
• Quality specifications and testing methods
• Identification and control measures for potential safety risk substances
Toxicological Safety Assessment
Assist in conducting required toxicological tests and preparing corresponding safety evaluation reports.
Efficacy Evidence Compilation
Collect and organize supporting data, including:
• Scientific literature and regulatory references
• In vitro/animal test results
• Human efficacy evaluation data
Technical Requirement Documentation
Guide the preparation of complete technical specifications for new ingredients.
Annual Safety Monitoring Reports
Assist in preparing mandatory post-market safety surveillance reports.
End-to-End Registration/Filing Agency Services
Provide full-cycle professional representation throughout the entire new ingredient registration/filing process.
