RAPS pre-approved webinar on "Improving Constraint Performance" from GlobalCompliancePanel
RAPS pre-approved webinar on "Improving Constraint Performance" from GlobalCompliancePanelme top portion of your press release.
- Wilmington, NC (1888PressRelease) October 03, 2012 - Constraints of one or another kind are inseparable from processes. In the medical device industry, when manufacturing intricate devices; constraints are natural barriers along the way.
How does a manufacturer eliminate these constraints? This is what this webinar will familiarize participants with. It will offer many ways of overcoming constraints in the manufacturing process. One of the theories the Expert of this webinar will present involves taking a fresh look at the Theory of Constraints.
This is how it works: Instead of taking the traditional route of assuming that an obstacle is a fixed entity; this approach looks at constraints as something that is dynamic and keeps adjusting itself to changing situations as they come by. Sidestepping the usual concept of expending resources and energies and focusing on the constraint, this approach hovers around the constraint and phases out some of the parts of it to non-constraint operations. It is somewhat like addressing the peripheries to eventually take care of the core. This makes the constraint look a lot less formidable, while paving the way for its easier resolution.
This is the outline of this webinar:
o Managing a constraint
o Identifying a constraint in a process by its symptoms
o How to increase the overall throughput of your production line
o The problem with measuring operator efficiency at the bottleneck
o Recognizing actions that do not need to be part of the constraint
o The nature of a constraint
When:October 3, 10:00 AM PDT | 01:00 PM EDT
By whom:
José Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For three decades, he has worked in the medical device industry specializing in manufacturing, process development, tooling, and quality systems.
His medical device experience includes surgical instruments, PTA & PTCA dilatation and guiding catheters, plastic surgery implants and tissue expanders, urology implants and devices for the treatment of incontinence, delivery systems for brachytherapy, orthopedic implants and instruments, and vascular surgery grafts and textiles.
Wherever he has worked, he has a track record of introducing world-class methodologies such as Kepner-Tregoe, Taguchi Techniques, Theory of Constraints, Lean Manufacturing, Five S's (Visual Workplace), process validation to GHSS standards, and similar approaches.
For whom:
The webinar will benefit
o Managers
o Supervisors
o Directors
o Vice-Presidents R&D
o Vice-Presidents Manufacturing Engineering
o Vice-Presidents Quality Assurance
o Vice-Presidents Operations
Duration: 60 minutes
To enroll for this webinar, contact
webinars ( @ ) globalcompliancepanel dot com
Phone: 800-447-9407
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