Omnex Resource Center

Automotive manufacturers are increasingly aware of the information security concerns associated with sharing intellectual property and domain expertise within their supply chain.

Publish Date:September 21, 2022

At the outset, there was no aerospace industry standard for APQP and PPAP; so Omnex was invited to join in the effort to develop a new approach to be deployed to the global aerospace supply base.

Publish Date:September 16, 2022

The increasingly software-defined vehicles in development today along with V2X communication and Over-the-air (OTA) communication, cybersecurity has become of central importance within automotive product design.

Publish Date:August 25, 2022

Automotive OEM’s are increasingly aware of the information security concerns associated with sharing intellectual property and domain expertise with their supply chain. Information security management, and ensuring adequate checks and balances on the information secure sharing networks have becom

Publish Date:August 02, 2022

To bolster information exchanges and data transfers, many organizations are requiring their external providers to implement an information security management system (ISMS) framework to achieve Trust Information Security Assessment (TISAX) maturity certification.

Publish Date:July 29, 2022

The aerospace Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP) standard, AS9145, was developed to leverage the successes found in the automotive sector.

Publish Date:July 21, 2022

The purpose of this Webinar is to introduce Reverse FMEA and show the steps required to perform, mitigate risk and report the results.

Publish Date:June 23, 2022

According to the US Department of Transportation's National Highway Traffic Safety Administration (NHTSA), less than 1% of vehicle crashes are attributed to vehicle failure (the domain of ISO 26262), and the remaining attributed to other reasons involving hazardous scenarios containing one or more .

Publish Date:June 21, 2022

The FDA regulatory requirement 21 CFR 820 for medical device Current Good Manufacturing Practice (CGMP) for Quality System Regulations (QSR) is undergoing a significant revision. The purpose of this webinar is to familiarize medical device manufacturers (marketing or intending to market in the USA),

Publish Date:June 14, 2022

Digitalization is the use of digital technologies to convert a process into digital information. The process performance turns into data that can be used to manage the process.The goal of digitalization is to reduce the number of steps in a process, reduce lead time, and to increase efficiency.

Publish Date:May 24, 2022