We advise international cosmetics brands, beauty businesses, formulators, manufacturers, importers, distributors and chemical companies on Italian and EU product compliance, market access, commercial contracts and regulatory incidents.
Discuss cosmetics or chemical compliancePlacing a cosmetic or chemical product on the Italian market requires more than a compliant label. The formula, safety assessment, Product Information File, Responsible Person, notification, manufacturing standards, claims, supply chain and incident procedures must support the same product story. We connect regulatory evidence with the contracts and controls needed to launch and keep products on the market.
We advise on the EU Cosmetics Regulation and Italian market requirements, including product classification, Responsible Person arrangements, CPNP notification, Product Information Files, Cosmetic Product Safety Reports, GMP evidence, ingredient restrictions, labelling, language requirements and substantiation of cosmetic claims.
We draft and negotiate formulation, manufacturing, testing, private-label, supply, import, agency and distribution agreements. We allocate responsibility for specifications, quality, regulatory documents, changes, audits, adverse events, withdrawals, recalls, stock and brand use.
For chemical products and ingredients, we assess REACH registration and supply-chain duties, safety data sheets, CLP classification, packaging and labelling, restrictions, advertising, distribution and product-liability exposure, coordinating technical specialists where scientific assessment is required.
We confirm whether the product is a cosmetic, chemical product or another regulated category, and identify the manufacturer, importer, Responsible Person, distributor, testing providers and target markets.
We review the formula, ingredient status, PIF, CPSR, GMP evidence, CPNP notification, artwork, mandatory label information and support for efficacy, natural, organic, dermatological and environmental claims.
We ensure manufacturing, private-label, import and distribution agreements define who controls specifications, notifications, quality records, product changes, complaints, adverse events, recalls, insurance and authority communications.
We assist with Italian market entry, distributor onboarding, post-market surveillance, corrective action, authority enquiries, product withdrawal, recall, consumer claims and disputes with commercial partners.
Before launch, the product generally needs an EU-established Responsible Person, a compliant safety assessment and Product Information File, CPNP notification, GMP-compliant manufacture and labelling that meets EU and Italian language requirements. The exact review depends on the formula, claims, supply chain and sales channels.
Yes. A cosmetic product placed on the EU market must have a Responsible Person established in the EU. The appointment should clearly allocate access to the PIF, notification, compliance checks, authority cooperation, adverse-event handling and corrective-action responsibilities.
We can review the legal completeness and consistency of the compliance package and coordinate with qualified safety assessors and technical specialists where scientific assessment is required. We also compare the file with the formula, artwork, claims and contracts.
Claims must be truthful, supported by adequate evidence and consistent with the product's actual function and regulatory classification. Particular care is needed for medicinal implications, before-and-after claims, dermatological statements, environmental claims, influencer content and comparative advertising.
Yes. We advise on contractual and regulatory issues involving REACH duties, supply-chain information, safety data sheets, restrictions, CLP classification, packaging and labelling. Technical testing and substance-specific scientific work can be coordinated with specialised consultants.
Yes. We help assess contractual and regulatory duties, preserve evidence, coordinate communications with the supply chain and authorities, review consumer notices and allocate the costs and responsibilities of corrective action, withdrawal or recall.
Share the formula, product file, artwork, claims and supply-chain structure. We will identify the Italian and EU cosmetics-law, chemical-regulation and commercial issues that should be resolved before launch or regulatory response.
Discuss cosmetics or chemical compliance