To celebrate the Coordinate Metrology Society 40th Anniversary, the CMSC is expanding its featured speakers to include 3 keynotes that have been recognized as “Titans” of the coordinate metrology industry: John Brown, Dr. Kam Lau, and John Palmateer. These individuals have a spent a lifetime involved in Coordinate Metrology and greatly advanced the science we all use daily. Each morning of the conference will include one keynote to discuss their area of expertise, how coordinate metrology has changed since 1984, and where the industry is going.
The Coordinate Metrology Society Conference (CMSC) is a major event for Measurement Technology Professionals. Established in 1984, the annual five-day conference showcases the latest in 3D technology and features engaging sessions with industry leaders. This year's event will mark the 40th Anniversary of the CMSC and will take place from July 22nd to July 25th at the Embassy Suites by Hilton Charlotte/Concord in North Carolina. Attendees can expect technical seminars, hands-on training sessions, interactive discussions, and networking opportunities with metrology professionals. Don't miss the opportunity to join us next July in Charlotte!
In theory, Control illuminates all aspects and in practice presents the current world range of usable technologies, processes, products and system solutions for industrial quality assurance.
This year the ASQ Inspection Division and the Greater Houston Section is having a joint conference on Quality: Then and Now, September 29 - 30, 2022 in Houston, TX.
The ManuSec USA summit is set in a world dominated by a focus on the Fourth Industrial Revolution, where manufacturers have increasingly adopted robotics, artificial intelligence, machine learning and advanced analytics.
Join manufacturing professionals from around the world at AI Manufacturing 2020, August 26-27 in Dallas, Texas, to discover integration strategies, ROI, and best practices.
The presentation will include: where GDP can be found in the CFR, We will discuss definitions of documentation, raw data, record keeping, and some do's and don't's.
The verification and validation of regulated software is coming under increased scruinty by the U.S. FDA.This webinar will address the use of the FDA, GAMP, 21 CFR Part 11,"Electronic Records"/"Electronic Signatures", IEC 62304, and other applicable industry software validation models, coupled with the ISO 14971/ICH Q9 Product Risk Management models, to plan, structure, run, and document acceptable software validations.