Cosmetics

Our Authorized Representative and Responsible Person services are designed to help cosmetic brands achieve fast, secure market entry with confidence. We provide expert, end-to-end guidance tailored to the unique regulatory demands of the beauty industry.
With over 37 years of experience, we support global compliance across the EU, UK, US, and beyond. Our services are backed by a trusted international network of regulatory specialists, ensuring your brand meets all requirements – wherever you choose to grow.

Select your region

We provide cosmetic regulatory support across the United Kingdom, European Union, and United States.

Our services cover key regulatory frameworks including the EU Cosmetics Regulation (EC) No. 1223/2009, UK Cosmetics Regulation, and relevant US requirements under MoCRA. We support brands in preparing for compliance by providing guidance on documentation, labeling, and market-specific regulatory expectations.

Whether you are entering a single market or managing compliance across multiple regions, our approach helps you understand requirements clearly and prepare your products accordingly.

European Union

The EU cosmetics market, serving over 450 million consumers, offers vast opportunities for growth but demands strict compliance with Regulation (EC) No 1223/2009 for market access.

United Kingdom

The UK maintains its high position in the global cosmetics industry with a dynamic market, requiring compliance with its own Cosmetics Regulation, including appointing a UK Responsible Person and submitting product data via the SCPN portal.

United States

The United States is one of the largest and most competitive cosmetics markets, requiring compliance with new MoCRA’s FDA rules.

One Partner for WorldWide Compliance

At Cert3Global, we provide structured regulatory support across the United Kingdom, European Union, and United States.

We support cosmetics and personal care brands in preparing for regulatory requirements in these key markets through clear guidance, documentation support, and coordination across applicable frameworks.

Whether you are launching a product for the first time or expanding into additional regions, our team helps you navigate regulatory pathways, understand market-specific requirements, and prepare for compliance.

Our approach focuses on clarity, accuracy, and practical implementation—supporting your expansion with a structured and informed regulatory strategy.

FAQs

Do I need a UK Responsible Person?
Yes, non-UK manufacturers must appoint a UK Responsible Person to place medical devices on the UK market.
UKCA marking confirms that a product complies with UK regulatory standards and is required for many products in Great Britain.n
Yes, medical devices must be registered with the MHRA before being marketed in the UK.n
It is a document confirming that a product is legally sold in the UK and meets regulatory requirements.n
Yes, we provide complete regulatory supportu2014from documentation to certification and ongoing compliance.n
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