MATERIALS METRIC ARCHIVES

July 29, 2026 by Materials Metric

Unknown compound identification | Materials Metric

Unknown compound identification turns mystery peaks into named structures. Materials Metric explains the analytical workflow behind it.

July 27, 2026 by Materials Metric

Choosing the right extraction conditions makes or breaks an E&L study. Materials Metric explains how to select solvents, time, and…

July 24, 2026 by Materials Metric

Exhaustive extraction captures the worst-case chemical profile of a device. Materials Metric explains when it beats simulated-use extraction.

July 23, 2026 by Materials Metric

Medical device extractables and leachables studies reveal what migrates from your materials. Materials Metric explains how E&L testing works.

July 22, 2026 by Materials Metric

Extractables vs leachables: what is the real difference and why it matters. Materials Metric explains how each study supports device…

July 21, 2026 by Materials Metric

Know your 510k testing requirements before you submit. Materials Metric outlines the data FDA expects for a clean premarket review.

July 20, 2026 by Materials Metric

A supplier change risk assessment protects you when materials shift. Materials Metric explains how to evaluate impact on device safety.

July 19, 2026 by Materials Metric

A material change biocompatibility re-evaluation is often required after substitutions. Materials Metric explains what triggers new testing.

July 18, 2026 by Materials Metric

Chemical characterization vs biocompatibility testing: which does your device need? Materials Metric explains how the two approaches work together.

July 17, 2026 by Materials Metric

Reusable medical device testing must account for cumulative exposure. Materials Metric explains how reprocessing changes biocompatibility needs.