Oxford Biosciences Cosmetic Product Experts Press Esc to close
Oxford Biosciences Cosmetic Product Experts Press Esc to close
Each market has its own framework. We prepare for all of them from a single evidence base, with the divergences treated explicitly.
Full EU cosmetic compliance under Regulation (EC) No 1223/2009: the Annex I CPSR, EU Responsible Person, CPNP notification, labelling and claims. Held on your behalf through our Irish-registered entity.
View requirements →Full UK cosmetic compliance: CPSR, SCPN notification, Responsible Person services, and Product Information File management. Led by a Clinical Pharmacologist with University of Oxford credentials. 100% acceptance rate.
View requirements →Cosmetic compliance across Central America under the COMIECO harmonised RTCA framework, whose annexes track the EU lists, with a single regional sanitary registration valid for five years. An EU-assessed product is a strong starting point.
View requirements →North American cosmetic compliance: US MoCRA safety substantiation with the state-level provisions, and Canadian Health Canada notification under the Cosmetic Regulations. Prepared by the assessor who signs our EU and UK CPSRs.
View requirements →Cosmetic compliance across South America: Brazil (ANVISA, RDC 907/2024), the Mercosur bloc (ANMAT and GMC Resolution 18/23), the Andean Community (Decision 833 and the mandatory sanitary notification) and Chile (ISP). Prepared from an existing EU or UK evidence base.
View requirements →Cosmetic compliance for the GCC (Saudi Arabia, the UAE, Bahrain, Kuwait, Oman and Qatar) under the harmonised GSO standards, with the national registration and Arabic-labelling requirements that differ between member states.
View requirements →Cosmetic compliance in North Africa, where Egypt (EDA, under Law 151/2019) and Morocco operate national frameworks closely modelled on EU cosmetic law. An EU-compliant dossier is a strong basis for entry.
View requirements →Cosmetic compliance across Sub-Saharan Africa, a fragmented landscape from mandatory NAFDAC registration in Nigeria and KEBS certification in Kenya to industry self-regulation in South Africa. We map an existing dossier onto each target market.
View requirements →Cosmetic compliance across the ASEAN member states under the ASEAN Cosmetic Directive: a harmonised technical baseline and four-part Product Information File, with country-by-country notification through NPRA, the Thai FDA, HSA, BPOM and the others.
View requirements →Cosmetic compliance in East Asia: China's CSAR registration and filing through the NMPA, Japan's quasi-drug line under the PMD Act, and South Korea's functional cosmetics under the MFDS. The most demanding regimes outside the EU and US, each needing an in-country representative.
View requirements →A technical reference on cosmetic regulation in China (CSAR/NMPA), Japan (PMD Act/MHLW), South Korea (Cosmetics Act/MFDS) and Taiwan (Cosmetic Hygiene and Safety Act/TFDA): classification, mandatory safety assessment, the domestic responsible entity in each market, ingredient inventories, and efficacy substantiation.
View requirements →Cosmetic compliance for Australia (AICIS under the Industrial Chemicals Act 2019, the Consumer Goods Information Standard 2020, and the TGA line) and New Zealand (the EPA Cosmetic Products Group Standard 2020, consolidated for 2026, with the PFAS phase-out).
View requirements →Cosmetic compliance in South Asia, led by India's Cosmetics Rules 2020: CDSCO import registration on Form COS-1 through the SUGAM portal, the perpetual registration certificate, BIS standard IS 4707, and the line between cosmetics and drugs.
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