Cosmetics Product Registration Services
Services We Offer
Cosmetic Product Registration & Approval Consulting
The registration process for cosmetics varies widely depending on the country and product category. Artixio’s experienced regulatory team ensures that your products comply with international regulations, from initial formulation to post-market surveillance.
We support cosmetic companies with product registration, safety assessments, and regulatory compliance consulting to meet global standards.
Cosmetics Product Registration and Approval Process
From compiling product dossiers to coordinating with authorities, our cosmetic regulatory consultants simplify approval and ensure label compliance.
Pre-Registration
- Assess ingredients and formulation for regulatory compliance
- Conduct safety assessments (e.g., toxicological reports)
- Prepare regulatory strategy and product dossiers
Registration
- Submit product dossiers and labeling to regulatory authorities
- Ensure compliance with regional regulations (e.g., EU, US FDA, ASEAN)
- Handle regulatory queries and documentation revisions
Post-Registration
- Ongoing compliance management
- Monitor post-market performance and reporting
- Support with renewals, variations, and claims compliance
Why Choose Artixio for Cosmetics Registration
- Compliance for 1000+ Cosmetics Product Licenses
- In-house Experts with 15-30+ Years of Experience
- Full Support from Concept to Market Launch
- Expertise in Global Cosmetic Regulations
- 5000+ Successful Product Approvals
- Strategic Solutions for Regional Requirements
FAQs
What documents are required for cosmetics product registration?
Do I need clinical trials for cosmetics registration?
Can Artixio help with cosmetics product labeling?
How do I maintain compliance post-registration?
Still Have Questions ?
Specialized Registration Services Across Multiple Industries
Pharmaceuticals
MedTech
Cosmetics
Nutrition
Biologics
Veterinary
Expert Regulatory Services To Streamline Compliance
Regulatory Intelligence & Strategy
Medical & Technical Writing
Publishing & Submission
Regulatory Affairs Across Multiple Countries
India
Singapore
Mexico
Brazil
Vietnam
Malaysia
Argentina
Colombia
Taiwan
China
European
Thailand
Indonesia
Philippines
USA
Japan
Qatar
South Korea
Insights from Artixio - Tips & Articles
Orphan Drug Designation in
Orphan Drug Designation (ODD) is regulated by Ministry of Food and Drug Safety (MFDS)...
Prioritizing Genes from Publicly
Artixio has developed an artificial intelligence based solution generating a list of prioritized genes...
CDSCO Simplifies Subsequent Importer
India’s regulatory authority, the Central Drugs Standard Control Organization (CDSCO), has published an important...