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  • 1 Request Info

    Webinar on Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration

    Overview: Design Inputs, Design Outputs, and Traceability matrices present a challenge to almost all industries that apply design controls. Typically, these cause the creation and maintenance of duplicate information across various documents - a major source of errors. This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to avoiding these errors, while presenting a fresh new approach to these key and related documents.
  • 2 Request Info

    Overlap between Engineering and Psychology - 2017

    Overview: This course will show how psychological factors enter into the engineering profession. Many aspects of the engineering profession are nontechnical such as balancing "green" practices with an effective cost structure, engineering ethics, how detail oriented should an engineer be, employee mental fitness for work, manager's leadership style, and communication between engineers. There will be at least one brief exercise that students will conduct on their own with guidance from the Instructor.
  • 3 Request Info

    Silica Exposure in the Construction Industry - New OSHA Regulations

    Overview Crystalline silica is a common mineral found in the earth's crust. Materials like sand, stone, concrete, and mortar contain crystalline silica. It is also used to make products such as glass, pottery, ceramics, bricks, and artificial stone. Silica is a mineral made up of silicon and oxygen, two of the most common elements on the planet. It comes in several forms, although by far the most common is crystalline silica. Crystalline silica is so abundant that it makes up over 12% of the earth's crust, making it the second-most common mineral on the planet.
  • 4 Request Info

    Critical Thinking, Problem Solving and Effective Decision Making

    Overview Every day at work, leaders are faced with many issues when making decisions. Some of our problems are big and complicated, while others may be more easily solved. There is no shortage of challenges and issues that can arise on the job. Critical thinking and problem solving are two essential skills that leaders need to have. Critical thinking refers to the ability to use knowledge, facts, and data to effectively solve problems. This doesn't mean you need to have an immediate answer, it means you have to be able to think on your feet, assess problems and find solutions. By learning how to strengthen your creative problem solving and decision making skills by breaking old habits, you will gain confidence and respect.
  • 5 Request Info

    Webinar On Lifecycle Approach to Analytical Methods: Incorporating QbD Principles into Method Development, Validation and Transfer

    This 90-minute webinar on using the Lifecycle Approach to Analytical Methods is designed to provide participants with a lifecycle approach to developing and validating analytical methods with improved outcomes for routine use and transfer.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/ANALYTICAL-METHODS-501375/MAY-2016-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On Comparability Protocols for Approved Drugs

    This webinar will address approaches to developing comparability protocols for approved drugs, including primary content considerations and timing of submission. The information obtained will enable completion of appropriate testing to make changes to the drug substance or drug product formulation, manufacturing facility, and container closure. The webinar will address aspects of preparing the protocol prior to confirmed changes in order to speed approval and preparing the appropriate updates to Module 3 of the CTD.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/COMPARABILITY-PROTOCOLS-APPROVED-DRUGS-501539/JUNE-2016-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On How to Integrate Culture during a Merger or Acquisition

    During a significant change like a merger or acquisition, listening, architecting and integrating both cultures are critical for maximizing the value of the deal. Organizations that thrive in today's complex environment benefit from dynamic, robust cultures. It is common knowledge that mergers often fail or fall short of realizing expected value due to complications during cultural integration. When surveyed, many CEOs reported that they had no plan in place for integration and even if they did, they wished in hindsight that they'd devoted more time and resources to cultural integration.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/INTEGRATE-CULTURE-MERGER-ACQUISITION-501566/JULY-2016-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On Human Factors/Usability Based on ISO 62366

    This training program will examine how human factors/usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process, and validating the effectiveness of the studies will be explained. The various types and methods of human factors analysis will be explained. This process conforms to the new ISO 62366 standard and the new FDA guidance document.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/HUMAN-FACTORS-USABILITY-BASED-ISO-62366-501460/JULY-2016-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Using Analysis of Variance(ANOVA) - A Practical Approach

    This webinar provides a powerful statistical tool called Analysis of Variance (ANOVA) that you can use to analyze data and improve processes. Because the tool is available in Excel, you don't need to purchase an expensive complicated software package. It is already available to you.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/USING-ANALYSIS-VARIANCE-ANOVA-501564/JULY-2016-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On Identifying and Addressing Cybersecurity Risks for Medical Devices

    Reports of cybersecurity attacks are appearing more and more frequently in the news affecting e-commerce, retail, the financial industry, the power grid, and in the healthcare setting. With more devices connected as part of the internet of things (IoT), the risks and number of potential threats increases exponentially. Connected medical devices present a unique set of risks due to the element of patient safety and potential for catastrophic outcomes.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/CYBERSECURITY-RISKS-MEDICAL-DEVICES-501617/JULY-2016-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On CE Mark - Required to Sell in the European Market

    Medical devices sold into the European Union (EU) must comply with the applicable medical device directives, EU laws similar to FDA's regulations. Medical devices declared compliant must bear a CE mark in order to be admitted into the 29 member countries comprising the EU.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CE-MARK-REQUIRED-SELL-EUROPEAN-MARKET-501636/AUGUST-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On FDA Regulation of Digital Health - Current Status and Recent Developments

    Why is the FDA focusing on Digital Health? Many medical devices now have the ability to connect to and communicate with other devices or systems. Devices that are already FDA approved or cleared are being updated to add digital features.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/FDA-REGULATION-DIGITAL-HEALTH-501646/AUGUST-2016-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Hazard Analysis following ISO 14971

    FDA expects that as part of a product development program risk management will be conducted. FDA recommends using ISO 14971 as a guide and has accepted it as a recognized standard. Hazard Analysis is the most powerful of the risk management tools described in ISO 14971 but it is very confusing. Many new concepts are introduced. We will explain these concepts and provide examples so that the process is clear.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/HAZARD-ANALYSIS-ISO-14971-501771/OCTOBER-2016-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Avoiding Common Mistakes in Medical Device Human Factors

    With the recent finalization of the FDA guidance, Applying Human Factors and Usability Engineering to Medical Devices, device developers have a clearer picture of the expectations for human factors testing on devices for which they seek clearance or approval. However, attempting to meet the FDA expectations using the guidance alone often results in limited understanding and poor execution of human factors studies.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/AVOIDING-MISTAKES-MEDICAL-DEVICE-501849/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach

    The various regulatory agencies have expectations that suppliers and vendors will demonstrate control over their manufacturing processes, validations, and documentation. Quality auditing is the process of checking whether these organizations have implemented what they have stated in written procedures and whether their people are doing what the organizations procedures state they will do.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/AUDITING-QUALIFYING-SUPPLIER-VENDOR-501737/DECEMBER-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Risk Management Using ISO 14971:2007 and EN ISO 14971:2012

    Risk management is essential to device design and required by other standards, such as usability engineering, biocompatibility and electrical safety. The basis is ISO 14971:2007, but many companies don't understand the standard, don't follow the process flow, and consequently don't have an effective implementation. This presentation helps you avoid the common problems and create a compliant system.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/ISO-14971-2007-501829/DECEMBER-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On Statistical Concepts of Process Validation

    If you conduct process validation, you need to ensure that your results are valid. Beyond the regulatory requirements, statistical approaches will help you achieve the desired result - processes that produce only conforming material. This presentation provides the background you need on the statistical approach to process validation.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/STATISTICAL-CONCEPTS-PROCESS-VALIDATION-501979/DECEMBER-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On How to Conduct a Human Factors Validation Test Following ISO62366 and the FDA Guidance

    Validation testing aims to show that a device can be used by the intended users without serious use errors or problems, for the intended uses and under the expected use conditions. This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/ usability validation test. HF/U validation is very different from device validation.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/HUMAN-FACTORS-VALIDATION-ISO62366-FDA-502041/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Quality by Design

    This webinar will help you learn the basics of design controls for medical devices. This webinar will focus on the fundamental concept that quality cannot be inspected in--it must be designed in. We'll cover the regulations and expectations for design control. We'll discuss how design control fits into your Quality Management System. Successful integration can enhance your new product development process.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/QUALITY-DESIGN-502012/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On BCBS 239 - Principles of Effective Risk Data Aggregation and Risk Reporting

    Risk management is a key component of every banking governance framework. This webinar discusses the BCSB 239 standard. The instructor will discuss the critical risk-data aggregation capabilities and internal risk-reporting practices (the Principles) to enhance risk management and decision-making processes at banks.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/BCBS-239-DATA-AGGREGATION-RISK-REPORTING-502031/FEBRUARY-2017-ES-TRAININGREGISTRY