
The IVDR transition: new duties for in-vitro diagnostic devices
Under the IVDR, most in-vitro diagnostics gained a risk class and a notified body they never needed before. See how reclassification and the timelines run.
Articles from our specialists on certification, testing, and inspection. Practical guidance on ISO management systems, CE marking, and food and sustainability certification, plus what the latest scheme changes mean for exporters.

Under the IVDR, most in-vitro diagnostics gained a risk class and a notified body they never needed before. See how reclassification and the timelines run.

ISO 14064 measures a company's annual emissions; ISO 14067 measures one product's footprint. See how the two carbon standards differ and when to use each.

A test measures a property; a certificate attests conformity. Learn which one your buyer is really asking for, when you need both, and how to sequence them.

What grocery retailers demand from private-label food suppliers: GFSI certification, technical and social audits, traceability, and how to win the listing.

A market-access guide to Gulf conformity: how UAE ECAS and EQM, Saudi SABER, the Kuwait report and the G-Mark decide what your product needs per market.

The EU Machinery Regulation replaces the Machinery Directive on 20 January 2027. See what changes for manufacturers, from the high-risk list to software and AI.

The same ISO 9001 findings surface in audit after audit. Here are the ten most common nonconformities, the clauses behind them, and how to prevent each one.

The EU MDR rewards the right order. How device makers sequence classification, ISO 13485, technical documentation, clinical evaluation and post-market work.

CBAM puts a carbon price at the EU border. See which Turkish exports are in scope, the key deadlines, and the verified emissions data your buyers now expect.