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MDlaw, COSlaw and PRODlaw are specialized regulatory intelligence platforms that centralize EU and international compliance requirements for medical devices, cosmetics, and consumer products. They provide instant access to MDR, IVDR, CPNO, EUDAMED, labelling rules, and national registrations, helping manufacturers, distributors, and Responsible Persons navigate complex legislations. Continuously updated, these platforms ensure business stay compliant, accelerate product registration, and reduce risks of market rejection or fines.

The most extensive & up-to-date information platform on the EU MDR & IVDR

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An extensive information platform on the global cosmetics regulations

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Electronics, Machinery, Construction, Toys, Motor vehicles & more

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FAQ

Frequently Asked Questions

Because it centralizes all EU and national regulations, helping manufacturers, Authorised Representatives, and distributors stay compliant and avoid missing critical updates.

MDlaw does not replace consulting but complements it. It gives regulatory teams quick access to verified legislative texts and guidelines, saving and reducing compliance risks.

COSlaw is a digital platform that centralizes EU and international cosmetic regulations, including Cosmetics Regulation (EC) No 1223/2009, guidance, CPNP requirements, and national rules.

Cosmetic manufacturers, Responsible Persons, importers, and legal teams managing multiple markets who need one reliable source for compliance rules.

PRODlaw is a regulatory platform covering a wide range of consumer products, from food supplements to chemicals, giving companies access to EU and national requirements. You can find legislations, compliance checklist, and official guidance for various product types.

Yes. By providing early visibility of new requirements and country-specific rules, they help companies adapt quickly and avoid costly non-compliance.

No. They provide regulatory intelligence and official documents, but are best used alongside expert consulting for tailored compliance strategies.

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