JH INTERNATIONAL / QUALITY & COMPLIANCE

OUR
COMPLIANCE

JH International plans and develops cosmetics manufactured in CGMP- and ISO 22716-certified facilities registered with the U.S. FDA. For the U.S. market, we support applicable cosmetic product listing; for the European Union, we prepare each product to meet the requirements of Regulation (EC) No 1223/2009, including a product-specific safety assessment. Our health supplements are produced in GMP-certified facilities in accordance with applicable food safety standards. Our skin care and cosmetic products undergo product-specific safety assessment and testing. We do not conduct animal testing at any stage of our cosmetics or health-supplement production. Where requested, we support halal-compliant production routes for suitable formulations.

European Union compliance illustration

European Union

We address product-specific EU compliance requirements for the intended market.

United States compliance illustration

United States

We coordinate applicable FDA and MoCRA registration, listing and documentation steps for the product.

Manufacturing practice compliance illustration

Manufacturing practice

Our cosmetics are manufactured in accordance with Good Manufacturing Practices (GMP) and ISO 22716 guidelines.

Korean requirements compliance illustration

Korean requirements

We arrange applicable Korean manufacturing and product documentation for the selected production route.

Special requirements compliance illustration

Special requirements

Where available, we can plan a suitable formulation and manufacturing route for halal certification.

WHAT WE CONFIRM

The right evidence
for each project.

Product categories, manufacturing facilities and target markets do not all share the same requirements. During development, we clarify which party is responsible for testing, registration or notification, labelling, claims and import procedures.

Facility certifications, product-specific claims and supporting documents are verified for each production site and final product scope. We do not present a registration, a quality standard or a facility credential as an approval of every product.

Need a specific certificate or document?

Tell us the sales country, product category and required evidence in your brief. We can then confirm availability and responsibilities before quotation or production.

DISCUSS YOUR REQUIREMENTS

START YOUR PRODUCT DEVELOPMENT

Tell us what you want to make.

Share your product category, market, quantity, target price, packaging direction and launch timing. We will review the brief and outline the next steps.

REQUEST AN OEM / ODM QUOTATION