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CTS, Sciemetric and innomatec have consolidated their Indian Sales and Support operations to now directly serve the country’s manufacturing and automation industries with the broadest leak test and in-process testing portfolio available in the market today.

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Here are 5 tips to help improve your production line in 2020. We want to help manufacturers identify their problem points on the line and identify ways modern manufacturing technologies can be applied to start seeing improvements in the short-term—without a massive overhaul. 

What does adding intelligence at the edge mean for manufacturing and industrial domains? Sciemetric's Product Manager, David Mannila, provides 7 tips and considerations for your line.

CTS, Sciemetric and innomatec have teamed up to offer the Indian manufacturing industry the broadest leak test and Industry 4.0 portfolio on the market. Learn more about the benefits this poses for manufacturing companies in India in this article for Industrial Product Review Magazine featuring Shankar Krishnamurthy, Vice-President and General Manager, Asia-Pacific operations.

In this webinar, Sciemetric’s Aaron Alberts shares his experience in helping world-leading manufacturers adopt in-process test (IPT) technology to improve defect detection, optimize cycle times and provide a more proactive response to production issues.

In this webinar, using examples of warranty return defects and QualityWorX data management and analytics software, Sciemetric’s Rob Plumridge will demonstrate how to use production data to quickly close the loop to find and fix the source of defects.

This blog post discusses how digital process signatures can be employed when a new quality problem crops up in the field, to identify the root cause and enable continuous improvement on your production line.

We talk about how Sciemetric’s new partnership with Cincinnati Test Systems (CTS) gives manufacturers worldwide access to the combined products and expertise of three world-leading masters of leak and other in-process test solutions.

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.