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Finite Element Analysis (FEA) is a powerful and well recognized tool used in the analysis of heat transfer problems. However, FEA can only analyze solid bodies and, by necessity thermal analysis with FEA is limited to conductive heat transfer. The other two types of heat transfer: convection and radiation must by approximated by boundary conditions. Modeling all three mechanisms of heat transfer without arbitrary assumption requires a combined use of FEA and Computational Fluid Dynamics (CFD).

Finite Element Analysis (FEA) has been an indispensable tool for design simulation for several decades but this wide spread use has been limited to simple types of analyses. Relatively recently, more advanced analyses have given easy-to-use interfaces enabling design engineers to simulate problems formerly reserved for analysts. FEA Beyond Basics targets the FEA users who wish to explore those advanced analysis capabilities. It will demonstrate how to move past the ubiquitous linear structural analysis and solve structural nonlinear problems characterized by nonlinear material, large displacements, buckling or nonlinear connectors.

ISO 14001:2015 is an environmental management standard (EMS) developed by the International Organization for Standardization (ISO). The ISO 14001 standard is generic and can be used for any organization, whether it provides physical products or services. The requirements must be carefully interpreted to make sense within a particular organization. Developing automotive products and the environmental impact of this activity is not like producing food products or offering consulting services; yet the ISO 14001 standard, because it is business and management oriented can be applied to any activity.

Leadership is about more than making effective strategic decisions for business outcomes. It is also about creating a positive workplace in which leaders can adapt to change and manage conflicts effectively. Leaders can build skills that can develop their presence by adopting the mindset of an improv actor. This means learning and practicing how to show up and be ready – ready to lead, to influence, and to contribute whether things go the way they are expected or not. And to have leadership presence: something that builds the trust we need to work together through good times and bad.

This self paced course reviews the important facets of ISO 9001:2015, the most widely accepted quality management standard.  The standard can be applied to any organization that, regardless of its type or size, needs to demonstrate its ability to consistently provide products and services that enhance customer satisfaction and provide assurance of conformity to customer and applicable statutory and regulatory requirements.  This four-hour ISO 9001:2015 is a high level review.

ISO 13485:2016 is an international standard that establishes the requirements for a quality management system specific to the medical devices industry. It specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services.

Global 8D (G8D) is a disciplined process developed by Ford Motor Company to help product development and manufacturing engineers identify and solve problems. Solving problems results in efficient, as well as effective, resolution to "root causes" of customer satisfaction issues, and helps reduce warranty costs. With this three-hour online course, you will learn the methods and tools used to complete each step in the Ford Global 8D find-and-fix problem-solving process, including steps to define the problem, verify the root cause and escape point, and prevent occurrence.

ISO 13485:2016 is an international standard that establishes the requirements for a quality management system specific to the medical devices industry. It specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services.

ISO 13485:2016 is an international standard that establishes the requirements for a quality management system specific to the medical devices industry. It specifies requirements for a quality management system, and how to demonstrate compliance to meet customer and applicable regulatory requirements. ISO 13485 is designed to be used by organizations involved in the design, production, installation, and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes.  Estimated to take up to 15-hours to complete.

The FDA requires employees to be trained in the current good manufacturing practice 21CFR210-211 as they relate to the employee's  functions to help assure the safety and efficacy of drug products. 

This interactive eLearning GD&T training course now utilizes HTML5 for better browser and device compatibility. It contains 23 robust, self-paced learning modules that explain the terms, symbols, modifiers, rules, and basic concepts of geometric tolerancing as prescribed in the ASME Y14.5-2018 Standard. Progress is easily measured with instant feedback throughout each lesson that reinforces and aids in concept retention, allowing the learner to determine where further review may be needed. Full color detailed animations that help participants clearly visualize concepts, along with audio narration and 3D solid part examples.

This self paced course reviews the important facets of ISO 9001:2015, the most widely accepted quality management standard.  The standard can be applied to any organization that, regardless of its type or size, needs to demonstrate its ability to consistently provide products and services that enhance customer satisfaction and provide assurance of conformity to customer and applicable statutory and regulatory requirements. 

ISO 14001:2015 is an environmental management standard (EMS) developed by the International Organization for Standardization (ISO). The ISO 14001 standard is generic and can be used for any organization, whether it provides physical products or services. The requirements must be carefully interpreted to make sense within a particular organization. Developing automotive products and the environmental impact of this activity is not like producing food products or offering consulting services; yet the ISO 14001 standard, because it is business and management oriented can be applied to any activity.

This self paced course reviews the important facets of ISO 9001:2015, the most widely accepted quality management standard.  The standard can be applied to any organization that, regardless of its type or size, needs to demonstrate its ability to consistently provide products and services that enhance customer satisfaction and provide assurance of conformity to customer and applicable statutory and regulatory requirements. Estimated to take up to 15 hours to complete,  this self paced course provides training on the standard, and how to lead or conduct internal audits and supplier audits using ISO 19011:2015.  

This interactive eLearning GD&T training course now utilizes HTML5 for better browser and device compatibility. It contains 29 robust, self-paced learning modules that explain the terms, symbols, modifiers, rules, and basic concepts of geometric tolerancing as prescribed in the ASME Y14.5-2009 Standard. Progress is easily measured with instant feedback throughout each lesson that reinforces and aids in concept retention, allowing the learner to determine where further review may be needed. Full color detailed animations that help particpants clearly visualize concepts, along with audio narration and 3D solid part examples.

This self paced course reviews the important facets of ISO 9001:2015, the most widely accepted quality management standard.  The standard can be applied to any organization that, regardless of its type or size, needs to demonstrate its ability to consistently provide products and services that enhance customer satisfaction and provide assurance of conformity to customer and applicable statutory and regulatory requirements.

ISO 14001:2015 is an environmental management standard (EMS) developed by the International Organization for Standardization (ISO). It’s a generic standard that can be used for any organization that provides physical products or services. ISO 14001 is the most widely used EMS because it’s both business and management oriented. However, the requirements must be carefully interpreted to make sense within a particular organization. For example, the environmental impact of developing automotive products is not the same as producing food products or offering consulting services, yet this standard can be applied to any of these activities.

Additive manufacturing (AM), is a manufacturing process of choice for functional part production, adding to the suite of choices a designer has available when designing a part for manufacturing. Like other traditional processes like casting and machining, AM has its set of constraints. An added layer of complexity comes from the fact that there are several different AM processes, and some of the design constraints are process-specific. On the other hand, AM offers a range of opportunities in design freedom and mass customization as well as in cost and lead time reduction in some cases.

ISO 14001:2015 is an environmental management standard (EMS) developed by the International Organization for Standardization (ISO). The ISO 14001 standard is generic and can be used for any organization, whether it provides physical products or services. The requirements must be carefully interpreted to make sense within a particular organization. Developing mobility products and the environmental impact of this activity is not like producing food products or offering consulting services; yet the ISO 14001 standard, because it is business and management oriented can be applied to any activity.

ISO 13485:2016 is an international standard that establishes the requirements for a quality management system specific to the medical devices industry. It specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services.