ISO standards

Compliance testing labs are where products prove they're ready for the real world — but what actually happens inside one? This primer walks through the key steps, tools, and methodologies engineers use to evaluate safety, performance, and regulatory adherence before products reach market.

Compliance engineering demands constant adaptation — and training is what makes it possible. This piece examines why continuous learning is essential for keeping pace with evolving standards, emerging technologies, and global regulatory requirements, and what it means for engineers who want to stay ahead.

Third-party test labs undergo rigorous ISO 17025 accreditation audits lasting days or weeks. Learn what auditors scrutinize—from equipment calibration to facility layouts—and why accredited labs provide manufacturers with the highest-quality compliance testing and reliable results.

The International Organization of Standardization (ISO) releases the third edition of ISO 15223 Part 1, for medical device labels.

ANSI has released a new edition of ISO 13485:2016, the standard for "Medical devices - Quality management systems - Requirements for regulatory purposes." The revised standard can now be purchased from ANSI's standards store.

The International Organization for Standardization (ISO) has released a new standard for "Small craft --...

TÜV Rheinland, a global leader in compliance testing and certification, announced its Systems Group...