The Virtual Approach to Expos in 2020 – Assembly Show Chicago October 27 – 28th

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The ASSEMBLY Show Virtual is the go-to resource for anything and everything related to assembly technology, equipment and products. The event will feature educational presentations lead by industry experts, new product demos, supplier information, numerous networking opportunities as well as the ability to live chat with attendees and schedule appointments.

The ASSEMBLY Show is the place to find innovative new ideas to help grow your business and career!

InterTech is attending the Virtual Expo where our leading leak test experts will be available for in-depth insights on the latest leak testing technologies.

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InterTech Development Company competence of testing and calibration laboratory ISO17025-2017 certification

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ISO/IEC 17025:2017 specifies the general requirements for the competence, impartiality and consistent operation of laboratories. ISO/IEC 17025:2017 is applicable to all organizations performing laboratory activities, regardless of the number of personnel.

Laboratory customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others use ISO/IEC 17025:2017 in confirming or recognizing the competence of laboratories.

InterTech has its certifications qualified until December 2023.

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Do you know whether to focus your efforts on improving your quality assurance or quality control system on key Medical Device Technology?

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When working through remediation efforts and your medical device malfunctioned during patient use, do you know whether to focus your efforts on improving your quality assurance or quality control system or decisions made on improvements be made to both?

Quality assurance and quality control have complementary functions and each carry responsibilities that serve very different purposes.

Without a clear understanding of these systems and how they should function, you’ll struggle to ensure your medical devices are safe and effective and meet the highest specifications requirements.

Review IDC design reports on key advances in the Medical Device Area particularly around recent Covid 19 technologies / know-how to gain understanding of the differences and cross overs of quality assurance and quality control and learn how to leverage the best tools and methodologies to successfully control and assure quality of your product and processes using leading edge InterTech technology and expertise.

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