EU & UK Cosmetic Ingredient Regulations: Latest Updates & Future Restrictions

Cosmetics

Upcoming Webinar

June 26, 2025

45 Minutes

Join the Webinar as per Your Time Zone

For the Americas, EU & Africa Region

 10:00 EDT | 9:00 CDT | 11:00 BRT | 16:00 CEST

For ROW 

18:00 AEST | 11:00 MSK | 16:00 MYT | 13:30 IST

Thank you for your interest in Freyr’s Webinar Series (FWS). We are excited to have you join us on June 26, 2025, for our session:

What is it all about?

In this focused session, we’ll provide a comprehensive overview of the latest developments in the EU & UK cosmetic regulatory landscape. We’ll cover recent updates to SCCS and SAG-CS opinions, UK Cosmetic Regulation Annexes, the current status of PFAS, and the future direction of SCCS. Stay ahead of evolving compliance requirements with actionable insights from our experts.

Latest SCCS and SAG-CS opinions on cosmetic ingredients in the EU and UK
Recent updates to UK Cosmetic Regulation Annexes
PFAS – What’s the current status and how does it impact your products?
SCCS future plans and the timeline for upcoming regulatory deadlines
Freyr’s Cosmetic Services Portfolio – How we can help with compliance and market entry

This session is a must-attend for anyone navigating the complex regulatory environment for cosmetics in the EU and UK!

Dorota Hinca is a professional Cosmetic Safety Assessor. With over 11 years of experience, Dorota has gained extensive expertise in various areas, including cosmetic product formulation, safety and efficacy testing, claims substantiation, and Regulatory Affairs. She has pursued her higher education in Cosmetic Chemistry. At Freyr, she is the Safety Assessor and Regulatory Affairs Specialist solely dedicated to the European Union (EU) and United Kingdom (UK) markets. In her day-to-day work, she helps clients ensure the safety of their products and comply with the ever-changing cosmetic regulations.

Maggie is EU/UK Safety Assessor and Delivery Team Lead at Freyr. Being an accomplished professional with over 8 years of expertise in the Cosmetics Regulatory Affairs sector, she specializes in European Union and United Kingdom Regulations. Holding degrees in Biotechnology and Cosmetics Chemistry, she brings multidisciplinary approach and extensive knowledge of dermato-cosmetic sciences, bolstered by postgraduate certifications in Safety Assessment. Trusted for providing expert advice targeted for EU and UK markets, she is a dynamic professional shaping the landscape of Cosmetics Safety and Regulatory Matters.

Antonio Catalano is a dedicated professional with over 15 years of experience in the Cosmetic Industry, specialising in regulatory affairs, marketing and innovation. As Technical Director, RA and QA Lead of a contract manufacturing organisation, he has managed the design, R&D and manufacture of a wide range of cosmetic, medical device and OTC products for markets in Europe, USA, China and the Middle East.

Holding an M.Sc. in Pharmaceutical Chemistry and Technology, an M.Sc. in Cognitive Systems and Interactive Media, and an MA in BIoethics, his work combines technical expertise with a strategic marketing perspective to ensure that products not only meet regulatory standards but also resonate with consumers. In Freyr he specialises in Product Compliance and CPSR safety assessments as Regulatory Affairs Manager, with a keen eye on product design and development.

Aspect	USA	EU	Australia	China	UAE
Regulatory Authority	FDA	EFSA & Member State Authorities	FSANZ	SAMR & NHC	ESMA & MOHAP
Major Regulation Governing Compliance	Federal Food, Drug, and Cosmetic Act (FFDCA); 21 CFR Part 110 (Current Good Manufacturing Practices)	Regulation (EC) No 178/2002 (General Food Law); Regulation (EU) No 1169/2011 on Food Information to Consumers	Food Standards Code (Australia New Zealand Food Standards Code)	Food Safety Law of the People's Republic of China (Revised 2015); GB Standards for Food Safety	UAE.S GSO 9:2017 (GCC General Requirements for Prepackaged Food)
Pre-market Approval Required?	No pre-market approval except for novel ingredients, color additives, or specific claims	No pre-market approval for general foods, but novel foods or health claims require EFSA approval.	No pre-market approval unless it's a novel food or makes health claims	Pre-market registration is required for novel foods, health foods, or products with new ingredients	Pre-market approval is required for certain foods, health products, and products with new ingredients
Processed Food Labeling Compliance /Labeling Requirements	Mandatory labeling as per FDA guidelines (Nutrition Facts, Ingredient Declaration, Allergens)	Must comply with EU Food Information Regulation (1169/2011); includes allergens, nutrition, and origin labeling.	Must follow FSANZ Food Standards Code for labeling; nutrition panels, allergens, and ingredient lists required	Must follow GB 7718-2011 (National Food Safety Standards) for labeling; mandatory nutrition facts, allergens, and shelf-life	Must follow GSO 9:2017 for pre-packaged food labeling; Arabic labeling, allergens, and nutrition facts required
Timeline for Registration	No fixed timeline: products can enter the market once compliant	No formal registration unless novel food; EFSA approval for health claims takes 12-18 months	No formal registration unless it's a novel food or makes health claims	Typically, 12-24 months for novel foods, shorter for regular processed foods	Approval may take 6-12 months for certain products. Regular processed foods can enter the market once label approval is obtained

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EU & UK Cosmetic Ingredient Regulations: Latest Updates & Future Restrictions