Learn the secret, frequently missing value in CoQ calculations, how to quantify conformance & non-conformance costs, ways to measure prevention, appraisal, and internal/external failure costs, why quality failures drain production capacity, and get tips for reducing CoQ in your facility.
Adam Doolhoff, Vice President of Research, Quality, and Innovation at Fresca Mexican Foods, discusses how unifying quality and production processes allowed his team to scale operations (to over 5 million tortillas daily) while maintaining an incredibly high standard of quality.
Auditing against a standard like ISO 9001 or one of the GFSI schemes isn’t easy and is rarely effective without the proper training, guidance, and tools. IJ Arora, CEO of Quality Management International Inc. (QMII) provides tips on the Internal Auditing process.
FSPCA Lead Instructor Christopher Snabes from TAG will review changes to the FDA Intentional Adulteration (IA) regulation, suggest several sure-fire ways to conduct your vulnerability assessments, discuss the 3 Elements approach, prepare you for Quick Checks.
Poor quality can waste 25%-35% of an organization's operating budget and cripple profitability. In this webinar on controlling costs of poor quality, Bill Levinson from Levinson Productivity Systems applies CoQ lessons from Ford, Franklin, Goldratt, and Imai to help manufacturers fix it.
What formula do leading manufacturers use to create process improvements that work … that actually stick? Join an experienced Ops leader as he shares how to create “sticky improvements” and uncovers obstacles that can prevent improvements from taking hold in your organization.
Why manufacturing leadership and operations are adopting a data-first approach instead of chasing digital transformation. Cam Bergen, CEO of Mode40, and Roger Woehl, CTO of SafetyChain, explain.
Learn how Blue Bell Creameries’ quality team uses customizable dashboards and digital forms to make data-driven decisions and optimize their quality programs.
For years, we've performed root cause analysis with whiteboards, Post-Its & spreadsheets using The 5 Whys, Ishikawa diagrams, FMEA, and DMAIC methodologies. Now, newer technologies have made the RCA discovery process faster and more precise, and support a direct link to CAPAs.
SafetyChain’s Kevin Lee discusses existing Root Cause Analysis methodologies and provides an inside look at modern technologies that are making RCA process easier and boosting yield.
To prepare you for a May 2021 implementation deadline, LeAnn Chuboff from SQFI explains what's changed in SQF Edition 9.0 and how to make your transition smooth.
Want to take control of your supplier network? Learn 5 steps that can improve your supplier ecosystem and help you get the best possible quality from your suppliers at the lowest risk.