Overview
Food supplements may require registration or notification depending on the health authority’s regulations. Maven has a thorough understanding of local laws and product classification to guide your product through the registration or listing process.
We compile all necessary technical documentation and verify administrative prerequisites such as local representation, health authority fees, timelines, and region-specific nuances.
Global Expertise
- USA: GRAS determination, Food Additive Petition, NDIN, DSHEA compliance
- EUROPE: Product classification, label and claims compliance, dossier submission
- INDIA: FSSAI product approval, food license, registration, formulation review
Advantages
- Cost-effective
- End-to-end Regulatory consultation
- Qualified team with hands-on experience across all FS&N categories
- Expert support for region-specific Regulatory complexities
- Interactions with Health Authorities (HAs)
- Structured approach to ensure quick product launch or market access
