Industrial Management

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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

    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.
  • 3 Request Info

    Lean Manufacturing Training

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. The Ultimate Improvement Cycle (UIC) integrates Lean, Six Sigma, and the Theory of Constraints into a combined strategy that will help you immediately focus your efforts on those areas that will make the greatest difference. This class presents basic laws of factory physics that show why the UIC delivers significant bottom-line improvement while other initiatives so often fail. It explains to you why focusing your efforts on apparent problems rather than systemic concerns is wasted effort. Cost of this course is $1,999.00.
  • 4 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.
  • 5 Request Info

    LEADERSHIP SKILLS FOR PRODUCTION SUPERVISORS

    To keep the production process running smoothly, industrial production supervisors must motivate and direct the employees they manage. This class teaches the skills a productions supervisor needs to know to successfully manage the production line. Cost of this course is $2,669.00
  • 6 Request Info

    SUPPLY CHAIN MANAGEMENT TRAINING

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. Effective development and management of your supply chain network will cut your costs and enhance your customer value through supplier relationship management. This is a sustainable source of advantage in today’s turbulent marketplace, where demand is difficult to predict and supply chains need to be more flexible as a result. The real competition today is not between companies, but between supply chains. The winning approach to supply chains is an integrated perspective that takes account of networks of relationships, sustainability, and product design, as well as the logistics of procurement, distribution, and fulfillment. Logistics and Supply Chain Management Training examines the tools, core processes, and initiatives that ensure businesses gain and maintain their competitive advantage. Cost of this course is $1,999.00.
  • 7 Request Info

    MRO PLANNING AND SCHEDULING TRAINING

    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 MRO 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 planning and scheduling in an MRO environment. 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 moves on to training in lean manufacturing, just in time (JIT), and the theory of constraints. The class finishes with a discussion of the latest MRO planning software and technologies. Cost of this course is $1,999.00
  • 8 Request Info

    LEADERSHIP ESSENTIALS FOR TEAM LEADERS & SUPERVISORS

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. In this Leadership Essentials course, you will learn how to establish direction for your team and to influence and align them toward the company's goals, motivating and committing them to action and making them responsible for their performance.
  • 9 Request Info

    Control Systems Technology - SCADA and PLC Training

    Case studies are used with examples of real world working SCADA and PLC systems in the water, electrical and processing industries.Get the latest developments in SCADA and PLC systems, fundamentals of their design, installation and troubleshooting.
  • 10 Request Info

    Exceptional Coaching and Team Building Skills

    Dr. Rick Goodman is a professional speaker, motivator, author and training consultant helping organizations Develop Great Leaders - Through Excellence in Communication, Team Building, Change Management, and Customer Excellence. Dr. Rick = RESULTS
  • 11 Request Info

    The New Supervisor: Sills For Success -In An Instant

    Learn how to develop leadership skills, make timely & effective decisions, effective communication, the use of praise, team building, manage conflict, and more. Enhanced IAI version comes complete with a DVD & reproducible post-test. 48 minutes
  • 12 Request Info

    Online Webinar on Traffic Flow Management - Managing ATC Congestion and Delays

    Overview: The topic starts with the communication system design that delivers the single ATCSCC facility with the radar and flight data from the entire National Airspace System (NAS) for real time processing and assessment. There is then a discussion of the various goals, strategies, and techniques the ATCSCC employs to manage and resolve areas of significant traffic congestion and delay. To draw the entire ATC series together, the webinar closes with an "end to end" flight scenario that starts with airline scheduling and asset management planning, followed by the step by step description of an aircraft flight from the initial receipt of the IFR clearance, through the taxi out, take-off, the TRACON experience, the enroute experience, followed by the arrival TRACON sequencing and, finally, the landing and taxi-in function.
  • 13 Request Info

    Laboratory Accreditation: Getting there is just the beginning

    Overview: Many laboratories struggle with developing and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs. Once accreditation has been achieved many laboratories have difficulty maintaining the QMS as evidenced by the number of non-conformances cited during the subsequent biannual audits. Areas Covered in the Session: Defining a Quality Management System (QMS) Management Components of a QMS Technical Components of a QMS Method Selection, Validation and Verification Ensuring analytical competency
  • 14 Request Info

    Seminar on Extracting information from geochemical data

    Most specialists strongly recommend to sample every meter of the drill core or of a trench and to use multielement analysis, rather than just asking the laboratory for gold test. There are also many other types of analysis that are ignored by the industry. But even when such analyses are requested, most of the time the fed geologist is not well trained on the necessary techniques and methods to extract all the information contained in the data. This seminar will teach you what to ask and how to extract all the important information of your data.
  • 15 Request Info

    Applied Statistics for FDA Process Validation 2017

    In Guidance for Industry Process Validation: General Principle and Practices, process validation is defined as, ""...the collection and evaluation of data, from the process design stage through commercial production.." The guidance further delineates the 'process design stage through commercial production' into three distinct stages of the product lifecycle: Stage 1: Process Design: The commercial manufacturing process is defined during this stage based on knowledge gained through development and scale-up activities. Stage 2: Process Qualification: During this stage, the process design is evaluated to determine if the process is capable of reproducible commercial manufacturing. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900806SEMINAR?channel=mailer&camp=Seminar&AdGroup=trainingregistry_April_2017_SEO
  • 16 Request Info

    Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices 2017

    The changing game for drug and device marketing, however, is governed by antiquated and inadequate rules created for traditional print and broadcast advertising by the Food and Drug Administration ("FDA"). How the FDA will deal with such advanced communication technology that can go "viral" and just as quickly disappear is the question that the industry is eager to have answered. The FDA regulates the promotion of prescription drugs, biologics, medical devices and biotechnology products to ensure that the information is not false or misleading. The FDA has for decades regulated traditional advertising for decades, published various guidance documents for industry and issued many violation letters. If the FDA determines that drug or medical device promotional material is false or misleading or lacking in fair balance as between benefits and risks, companies could be forced to implement costly corrective actions, such as remedial advertising, suffer damage to their reputations
  • 17 Request Info

    Applied Statistics for Scientists and Engineers

    Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting validation criteria and specifications, performing measurement systems analysis (MSA), conducting stability analysis, using design of experiment (DOE) for process development and validation, developing process control charts, and determining process capability indices. Different statistical methods are required for each of these particular applications. Data and tolerance intervals are common tools used for setting acceptance criteria and specifications. Simple linear regression and analysis-of-covariance (ANCOVA) are used for setting expiries and conducting stability analysis studies. Two-sample hypothesis tests, analysis-of-variance (ANOVA), regression, and ANCOVA are methods used for analyzing designed experiment for process development and validation studies. Descriptive statistics (distribution
  • 18 Request Info

    Background Checks, Criminal Records and Safe Hiring 2017 Effective and Compliant Program 2017- Before 30 April 50% Discount for its All Seminars

    Employee problems are caused by problem employees, and this session will help HR professionals legally avoid bad hires in the first place. Just one bad hire can result in a legal and financial nightmare. Without taking appropriate steps, there is a near statistical certainty that an employer will hire someone with an unsuitable criminal record, or a falsified background, that can result in workplace violence, lawsuits for negligent hiring and time wasted recruiting and hiring the wrong person. On the other side of the screening fence, are the rising tides of lawsuits against employers alleging screening methods violate the law or are at odds with changes in civil rights legislation and the new EEOC Guidance on the use of criminal records. The screening landscape is more complex than ever. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900916SEMINAR?trainingregistry_SEO
  • 19 Request Info

    Medical Devices Industry and Risk Management 2017-Before 30 April 50% Discount for its All Seminars

    Gaps, incorrect or incomplete implementation of software can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all necessary steps to design, implement and test critical medical device software in a regulatory compliant environment. Software risk management has to be embedded into the bigger scope of overall risk management. Therefore this course will additionally address the system level risk management and the resulting interfaces to software. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900888SEMINAR?trainingregistry-SEO
  • 20 Request Info

    The EU General Data Protection Regulation (GDPR) 2017

    On 25th May 2018 the EU-GDPR becomes effective, this date has been set to give organisations time to prepare and comply with the regulations. This may seem to be a long way off, but for most organisations there is a lot to be done. With the escalation of data breaches, the sooner data is safe guarded the better. Often a data breach is not discovered for months, sometimes six months, implementing new policies, security systems, negotiations with suppliers and training people in an organisation will take time. The sooner you start the more time you have to make a good decision on the options you face. This introductory course will give you an overview of the history of Data Protection within the EU and introduce you to the enhancements and new obligations imposed by the EU GDPR Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901168SEMINAR?trainingregistry-September-2017-SEO