GMP & ISO Lab Consulting
for European Companies

Our Mission: Helping European Companies Export with Confidence

Care Europe was founded to solve a specific problem: European manufacturers — cosmetic brands, supplement producers, contract labs — have excellent products and strong EU compliance, but face a complex and unfamiliar regulatory landscape when they try to export to the USA or Canada. FDA cGMP requirements, 21 CFR Part 111, Health Canada's NHPD framework, and ISO 17025 export documentation standards are fundamentally different from what European companies are used to.

GMP & ISO Analysis for Export-Ready Documentation

We help European companies perform GMP-compliant analysis and prepare the ISO-aligned documentation that US and Canadian regulatory authorities and buyers expect. Whether you need a Certificate of Analysis in FDA-compliant format, a GMP audit readiness assessment, or guidance on how your EU ISO 22716 cosmetics GMP maps to US cGMP expectations — Care Europe provides the expertise to bridge that gap.

Registered and Operating in France

Care Europe is an officially registered French business. Our bilingual EN/FR capability means all regulatory reports, export dossiers, and compliance documentation can be prepared in both languages — essential when communicating with European labs and North American regulatory authorities or buyers.

Part of the Qalitex Group

Care Europe is part of the Qalitex Group — a network of laboratory and regulatory consulting businesses spanning North America and Europe. European clients benefit from direct access to ISO 17025 accredited laboratory testing through Qalitex (USA) and Androxa (Canada), giving them a complete EU-to-North America compliance and testing solution.