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Monitoring with Process Signature Analysis

  • Article in MDDI
October 26, 2010

Process signature verification helps medical device manufacturers eliminate destructive testing, bring more accuracy to the manufacturing process, and reduce costs. Rather than subjective post manufacturing quality control approaches, such as visual testing, or statistically based tests, like destructive testing practices or auditing, comprehensive process signature verification provides actionable insight into manufacturing processes as well as a wealth of data that can prove compliance with internal directives and FDA regulations.

In-Process Gaging is Cost Effective

  • Article by SME
July 1, 2010

Sciemetric CEO Nathan Sheaff discusses with the editors of Manufacturing Engineering magazine the company’s early successes with Ford Motor Co. in using digital process signature analysis to monitor quality on an engine as it was being built versus waiting for the end-of-line hot test.

Movers & Shakers Interview

  • Article by Frost & Sullivan
March 3, 2010

Sciemetric CEO Nathan Sheaff and Director of Sales Ron Pawulski are featured in a Movers and Shakers interview with market research firm Frost and Sullivan about the company, its markets and its prospects.

The Latest on Leak Detection

  • Article in Assembly Magazine
November 19, 2009

Sciemetric’s sigPOD is featured by the editors of Assembly Magazine as part of a roundup on the latest leak test systems on the market from a number of competing vendors.