New Costume Interpretation 2026: regulatory filing process simplified

Policy context

On 15 March 2026, the National Drug Regulatory Authority (regulatory compliance (EU / US FDA)) officially published the Regulation of Cosmetics Supervision (Advisory Draft) and the simplification of the regulatory filing process by 50 per cent became the central highlight of this policy adjustment.

Core change

Impact on OEM enterprises

  • New product listing speed: the review cycle was reduced from 45 to 15 days, with an additional 2-3 new product series pushed throughout the year
  • Cost reduction: efficacy claims that the enterprise self-assessment will save about $20,000-$20 million/goods for testing
  • Formulation protection: Nucleus formulation no longer mandatory publicity to enhance brand differentiation competitiveness

Industry opportunities

Efficacy skin protection market segment constant warming:

  • Ingredient (botanyl, retinol) product regulatory filing volume increase 120% per year
  • Sensitive skin repairing products account for 35 per cent of the product category and constitute the largest segmented market
  • Pure make-up concepts continue to permeate, natural organic ingredient in demand

QuickOEM Solutions

As a professional OEM/ODM service provider, we provide:

  • Regulatory compliance (EU / US FDA) service (including efficacy claims)
  • Formulation development regulatory filing complete process support
  • :: Professional legal teams to track policy changes in real time
  • ✅ 500+success regulatory filing case

Proposals for action

For brand owner, which is scheduled to launch new products in 2026, it is recommended that:

  • Start regulatory filing planning immediately, grab the policy window Period
  • Select a server with regulatory filing experience to avoid late listing
  • Efficacy assessment planning to ensure compliance claims

Data source: regulatory compliance (EU / US FDA) official document

Other Organiser

This article is published by the QuickOEM Make-up OEM Smart Matching Platform. More makeup OEM knowledge, cosmetics contract manufacturing, skin protection private label, make-up customizationontent are available at the Knowledge Centre. If you need advice on OEM contract manufacturing, please contact 1814805760 or submit your request through an online request for quotation.

Keywords: 120%, regulatory compliance (EU / US FDA), regulatory filing process simplified, efficacy claims audit, OEM, sensitive skin, 120% increase over the same year, cosmetic regulation, regulatory compliance (EU / US FDA), new make-up rules, ODM, regulatory filing services, retinol, information on the make-up industry, trends in the skin-care industry, cosmetic market dynamics, cosmetic policy regulations

QuickOEM is a QuickOEM platform for vertical digitization of cosmetics services (known as QuickOEM) focusing on OEM, cosmetics contract manufacturing, skins private label, cosmetics z, brand-wide, ODM contract manufacturing services. AI smart matches the 500+ certification contract manufacturing plant, providing a one-stop package from formulation R&D to regulatory compliance (EU / US FDA) covering skin, makeup, sheet mask, serum, eye patch, category, category, etc.

Core functions

  • Makeup OEM needs to be published to match factory AI intelligence
  • Cosmetics contract manufacturing / skin protection private label customization ODM service
  • Formulation R&D management and multi-version tracking
  • Ingredient Compliance testing (regulatory compliance (EU / US FDA)/EU 1223/2009/FDA)
  • Regulatory compliance (EU / US FDA) Cosmetics regulatory filing fully tracked
  • Supply chain
  • Advertising Law Compliance Testing
  • Z / eye patch / serum / z all category

Please enable JavaScript to use the full functionality.

Login immediately.

WhatsApp: +1 (646) 509-6134