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Courses

  • 1 Request Info

    Inventory Management

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. No business can survive very long without an effective program of controls over the parts and materials used in producing or distributing the goods and services of the firm. Three day class. Cost is $1999.00.
  • 2 Request Info

    Facility Management

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. This course is for those who not only want to obtain a thorough understanding of the methods, skills, and equipment used in the art of facility management, but also seek firsthand knowledge on how to manage effectively in a changing world. Three day class. Cost is $1999.00.
  • 3 Request Info

    PRODUCTION PLANNING

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. Students are taught how to create a process map to help enable them to identify problems with a particular production line. The class then takes an extensive look at forecasting to provide students with an understanding of industry recommended procedures for reliable forecasting. Next, we examine best practices in sales and operations planning and preparation of the master schedule. We now discuss best practices in materials resource planning (MRP), capacity management, and production activity control to learn how to make the most of what we have to work with. The class finishes up with training in lean manufacturing, just in time (JIT), and the theory of constraints. Cost of this course is $1,999.00
  • 4 Request Info

    WAREHOUSE MANAGEMENT

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. This three day class unravels the secrets of those best-in-class operations and shows how they create a competitive advantage for their companies. The class starts by analyzing the current state your operations; based on the results, the class provides a systematic, yet flexible, action plan for improvement, which involves human behavior, process redesign, warehouse management systems, and supply chain alignment. Class materials, along with case studies, detailed examples, and thought provoking questions will move your facility to best-in-class. Cost of this course is $1,999.00.
  • 5 Request Info

    SIX SIGMA TRAINING

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. Six Sigma has taken the corporate world by storm and represents the thrust of numerous efforts in manufacturing and service organizations to improve products, services, and processes. Although Six Sigma brings a new direction to quality and productivity improvement, its underlying tools and philosophy are grounded in the fundamental principles of total quality and continuous improvement that have been used for many decades. Nevertheless, Six Sigma has brought a renewed interest in quality and improvement that few can argue with, and has kept alive the principles of total quality developed in the latter part of the 20th Century. This three day class shows students the essence and basics of Six Sigma, as well as how Six Sigma has brought a renewed interest in the principles of total quality to cutting-edge businesses. Cost of this course is $1,999.00.
  • 6 Request Info

    Inventory Management Techniques: Planning, Replenishment and Activities Control

  • 7 Request Info

    Lean Manufacturing: Doing More And More With Less And Less

    Learn how to turn operations into an effective tool to compete in today's marketplace by becoming faster and more responsive to customer demand! Help your company do more--more rapidly--with fewer resources, less risk, less investment and less effort.
  • 8 Request Info

    Best Pratices in Strategic Outsourcing: It's Not Just for Manufacturing Anymore

    Attend this seminar and understand all facets of outsourcing as it applies to supply chain management. Find out how and where to start and the short- and long-term benefits for your organization—including immediate cost reductions and process improvement.
  • 9 Request Info

    AB RSLogix PLC Training Seminar - St. Louis

    Hands-On PLC Training Workshop (PLC: Programmable Logic Controllers). Start with basics move on to troubleshooting, then learn the foundations of good PLC programming while writing your first IEC-1131 compliant PLC program. (1.6 CEU) If you would like to learn how to reduce downtime thru PLC training, please sign up immediately for our 3 day workshop in Saint Louis. (As there is limited seating and these fill up quickly.) Bonus: In addition to every attendee being sent home with extra PLC learning material ... as an additional bonus, we give every attendee our RSLogix 5000 PAC training software for free too! No other provider can come close to the value of this PLC training workshop! So register soon.
  • 10 Request Info

    PLC Training

    Business Industrial Network provides Allen-Bradley Programmable Logic Controller (PLC) troubleshooting training. (1.6 CEU for on-site and Seminars)PLC Training CBT CDs also offered. Now also free PLC, Trainer, RSLogix 500 simulation software and free RSLogix 5000 training software to every attendee. No one else comes close to matching the value we offer.
  • 11 Request Info

    PLC troublshooting Training

    Hands-On PLC Training Workshop (PLC: Programmable Logic Controllers). Start with basics move on to troubleshooting, then learn the foundations of good PLC programming while writing your first IEC-1131 compliant PLC program. (1.6 CEU) Now also free RSLogix 5000 training software to every attendee. No one else comes close to matching the value we offer.
  • 12 Request Info

    An Advanced Course on Lean Documents, Lean Configuration and Document Control

    In this Lean Documents, Lean Configuration, and Document Control training learn the different types of lean documents and the usage of lean document principles; types of controlled documents; examples of lean and non-lean controlled documents. Pros and cons of lean vs. non-lean documents. Just as a manufacturing process produces a product, controlled documents are the product of a business process. Just as in manufacturing, a product cannot move forward if it is waiting for component parts, a document cannot move forward if it is waiting for information, or if its use is constrained by other documents. Although many life science companies advocate lean manufacturing, lean laboratory, and lean operations, they have cumbersome controlled documents and systems which cause significant operating expenses, and make it difficult to introduce process improvements in a timely manner.
  • 13 Request Info

    Verification vs. Validation in Regulated Industries by John Chapman

    Areas Covered in the Webinar: Verification & validation types. Definitions. Design control. Process control. Application. Consequences of poor verification & validation. Why verification & validation makes good business sense?
  • 14 Request Info

    Lean Basics

    This online course identifies lean principles for use in organizations looking for culture change. Implement lean strategies and streamline workflow with this great tool for project managers.
  • 15 Request Info

    Supply Chain Management Basics

    This online course provides users with the tools to appraise vendors and suppliers, source goods and services in a global economy, and maintain an effective supply chain with minimal interruptions.
  • 16 Request Info

    Empowering Employees

    Learn what empowerment really means and how it can help your company, the six key factors needed to empower your employees and motivate them for success, what really motivates your employees and when and how to provide needed feedback.
  • 17 Request Info

    Seminar on Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)- Before 30 April 50% Discount for its All Seminars

    This workshop style training course is supported by comprehensive knowledge of U.S. FDA laws and regulations and 30 year of extensive experience working within in the U.S. FDA regulated industries. In these 2 days, the following essential topics will be covered: Total Product Life Cycle and Your Medical Device An Overview of U.S. FDA Medical Device Regulation Regulations for Design and Product Development Premarket Notification - 510(k) and Premarket Approval (PMA) Regulations for Production & Process Control Readiness for FDA Facility Inspection Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900772SEMINAR?trainingregistry_SEO
  • 18 Request Info

    Audit Like the FDA - How to develop and implement an efficient and effective audit program

    This 2 day seminar will explore how to create and implement an efficient and effective internal audit program. Internal Audit is a required part of an effective quality system. More importantly, it is an incredibly powerful tool to identify areas of non-compliance. A well-designed audit program can be an effective tool in understanding, communicating, and reducing quality and compliance risk. However, estimates indicate that up to 75% of companies conduct audits only because they are required to by regulation. Businesses often see internal audit as a non-value added activity leading to meaningless findings, bureaucracy, and cumbersome processes. And despite having an internal audit program, management is often surprised when they receive a 483, Warning Letter, or even a Consent Decree. A well planned audit program can reduce these risks.
  • 19 Request Info

    Statistical Process Control -verification, validation, risk management, Manufacturing, and QA/QC 2017

    The 2-day seminar explains how to apply statistics to manage risks and verify/validate processes in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry. The flow of topics over the 2 days is as follows: ISO standards and FDA/MDD regulations regarding the use of statistics. Basic vocabulary and concepts, including distributions such as binomial, hypergeometric, and Normal, and transformations into Normality. Statistical Process Control Statistical methods for Design Verification Statistical methods for Product/Process Qualification Metrology: the statistical analysis of measurement uncertainty, and how it is used to establish QC specifications How to craft "statistically valid conclusion statements" (e.g., for reports) Summary, from a risk management perspective
  • 20 Request Info

    FDA's Latest Regulations for Computer Systems Used in the Tobacco 2017

    The Tobacco Control Act went into effect by FDA on June 22, 2009. Through this ruling, the FDA regulated cigarettes, cigarette tobacco, roll-your-own tobacco and smokeless tobacco, but in 2016, the FDA finalized a rule, Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act, which extends the FDA's authority to include the regulation of electronic nicotine delivery systems (such as e-cigarettes and vape pens), all cigars, hookah (water pipe) tobacco, pipe tobacco and nicotine gels, among others. The rule went into effect on August 8, 2016.