Regulatory Classification & Market Access Diagnostic

• Applicable framework determined from the composition, uses and claims
• Obligations to examine for the chosen market
• Risk of biocidal qualification
• Roadmap

• Complete quantitative composition (%)
• Intended uses and claims
• Raw material SDS (if available)

• Product authorisation
• Complete dossier
• SDS authoring (on quote)

• 1 round of written questions included
• A package covers one product and one defined market. A formula change, a new variant or a new market requires a new quote.
• The final check covers the requested corrections, on a consolidated version sent within 30 days. It does not cover a new creation.
• Turnaround from a complete file, subject to confirmed capacity. No administration or third-party laboratory timeline is guaranteed.
• If your file falls outside the package, I send you a quote, without charging the unsuitable package.
• All analyses are carried out by Justine Teruel.

Regulatory consulting and documentation preparation — not a certification and not a notified body. Bridge & Flow prepares Part A of the cosmetic product safety report (CPSR); Part B (assessment and signature) is the job of a qualified safety assessor, who may be a toxicologist colleague brought in on quote. Bridge & Flow acts as EU Responsible Person (Reg. 1223/2009) only under its dedicated service, on quote and under a separate written mandate. Where included in the service, Bridge & Flow may prepare and carry out an administrative submission on behalf of the legally responsible entity, subject to the required authorisation, access and information. This alone does not make Bridge & Flow the Responsible Person, importer, downstream user or other legal duty holder.