How can you ensure your products conform to EU rules? How can you carry out a conformity assessment? Presumption of conformity, harmonised standards, notified bodies, NANDO database.

Learn about the EU declaration of conformity, who must sign it, what information to include, language and translation requirements and how to keep it up to date.

From the 12th of August this year, all packaging sold in EU markets will be legally required to have its own PPWR-related ...

Many facets of our daily lives depend on standards. Standards influence the products we use, the foods we eat, how we communicate, our means of travel, our modes of work and play, and many other ...

STOCKHOLM, Sweden--(BUSINESS WIRE)--atsec is thrilled to announce it is the first accredited conformity assessment body (CAB) for the new EU Common Criteria (EUCC) certification scheme. With this ...

Conformity assessment refers to any activity designed to confirm that a product or service meets requirements contained in a specification (typically a standard). A specification is the technical ...

For medical device manufacturers targeting the European Union market, compliance with the Medical Device Regulation (MDR) is ...

Australia’s Therapeutic Goods Administration posted a proposed rework of the agency’s conformity assessment procedures that would align with EU regulations, but the agency stated clearly that it is ...

NABL revises assessment framework to introduce midcycle review and risk-based surveillance: Shardul Nautiyal, Mumbai Tuesday, ...

The U.S. FDA’s Accreditation Scheme for Conformity Assessment (ASCA) program is one of a number of efforts on the agency’s part to reduce the drag on premarket medical device submissions, but the ...

*This article was updated to specify the scope of the conformity assessment procedure. The EU lawmakers leading on the AI Act have circulated revised compromise amendments on how AI systems that could ...