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  • 1 Request Info

    Webinar on Reliability Engineering Fundamentals for Medical Devices

    This webinar will cover the science and techniques for designing highly reliable medical devices at lower cost and in lesser time. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Reliability-Engineering-Fundamentals-for-Medical-Devices-503951/JULY-2018-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on Fundamentals of Reliability and Safety Engineering for Medical Devices-Webinar Series

    Attend this webinar series by expert speaker Dev Raheja, to get complete guidance on Fundamentals of Reliability and Safety Engineering for Medical Devices. Price:$500.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Fundamentals-of-Reliability-and-Safety-Engineering-for-Medical-Devices-Webinar-Series-504744/JULY-2018-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on How Lock Out/Tag Out (LOTO) Can Prevent Accidents and OSHA Penalties for Non-Compliance

    Join LOTO standard webinar with John J. Meola to learn OSHA's zero energy assurance standard lock out/ tag out procedure. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/How-Lock-Out-Tag-Out-LOTO-Can-Prevent-Accidents-and-OSHA-Penalties-for-Non-Compliance-504133/JUNE-2018-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Emergency Preparedness: What Does Cal/OSHA Require?

    Develop an emergency action plan that protects employees from disaster and your company from Cal/OSHA citations and fines. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Emergency-Preparedness-What-Does-Cal-OSHA-Require-502454/MAY-2018-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar on FDA's Medical Device De Novo Reclassification Process

    This webinar will examine and define De Novo and discuss the key elements of this classification process. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/FDA-s-Medical-Device-De-Novo-Reclassification-Process-502304/MAY-2018-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar on Key Tips For Engaging Adult Learners

    This webinar tells how to design and deliver training in a manner that can successfully motivate audience - adult learners - to engage in the learning process. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Key-Tips-For-Engaging-Adult-Learners-507791/MAY-2018-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar on Discussion on Raw Material Methods and Specifications (Active and Inactive Ingredients) Referenced in UPS, EP, and JP Compendia

    The webinar on Raw Material Methods discusses how FDA has approved hundreds of inactive ingredients for thousands of products with various dosage forms. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Discussion-on-Raw-Material-Methods-and-Specifications-Active-and-Inactive-Ingredients-Referenced-in-UPS-EP-and-JP-Compendia-509975/MAY-2018-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar on GMP Complaint Systems, FDA's Adverse Event Reporting & Product Recalls

    Gain a clear understanding of what FDA inspectors look for when evaluating complaint handling and medical device reporting programs. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/GMP-Complaint-Systems-FDA-s-Adverse-Event-Reporting-Product-Recalls-502220/APRIL-2018-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar on Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success

    Training program on onboarding process in GMP environment. Learn how to differentiate the training requirements for full-time employees and contractors. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Onboarding-Employees-in-a-GMP-Environment-Best-Practices-for-Foundational-Employee-Success-506161/APRIL-2018-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar on Risk Management - Utilizing Lean Documents and Lean Configuration

    Attend this webinar to know the theory of lean documents and lean configuration to present a fresh approach to linked and cascading documents, files, and requirements. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Risk-Management-Utilizing-Lean-Documents-and-Lean-Configuration-507585/APRIL-2018-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar on Acceptance Activities in FDA's Quality Management System

    Understand how purchasing and acceptance activities are linked and combine to facilitate effective supplier management Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Acceptance-Activities-in-FDA-s-Quality-Management-System-507314/APRIL-2018-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar on Understand New 20 CFR 1926 Subpart AA - Confined Spaces in Construction

    Learn in detail about OSHA's final rule regarding confined spaces for construction and General Industry. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/OSHA-Confined-Space-Entry-Training-for-General-Industry-and-Construction-509616/APRIL-2018-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar on Designing and Using KPIs and Performance Dashboards

    Designing, developing and supporting an effective reporting system of leading and lagging KPIs (Key Performance Indicators) is complicated. Information needed by senior management is different and less granular than that needed by the line managers and the producers. The technical aspects of pulling the right information from the mountains of data at the right time can be overwhelming. We can help demystify this puzzle and put your team on the track to smooth sailing. Join us and accelerate your team’s understanding and effectiveness in designing, implementing and monitoring critical KPIs using powerful performance dashboards. Learn how to tailor your dashboards to perfectly fit the needs of your C-suite, middle managers and line and field personnel. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Designing-and-Using-KPIs-and-Performance-Dashboards-50
  • 14 Request Info

    Webinar on Creating a Good Design History File (DHF) for Audit Success

    This webinar will cover the basics on how to maintain a good Design History File (DHF) that will help a manufacturer in a regulatory compliance audit. The webinar will cover the structure of a DHF and steps to ensure that the DHF is completed as the design and development process progresses. The DHF needs to be maintained as design changes are performed. Information in the DHF can help facilitate design decisions, which often can affect the safety of the device. The DHF provides the knowledge base needed for the manufacturer to maintain the device. It also provides the secrets to a successful Design Control audit. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Creating-a-Good-Design-History-File-DHF-for-Audit-Success-506030/MARCH-2018-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar on Developing an Effective Risk Management Plan for Medical Devices

    This presentation gives you the essential information to write a successful Risk Management Plan. Don't skip required items or add additional, but unnecessary information. If the item doesn't apply, so why. Don't include extraneous information such as market size and share; they are not relevant. The Risk Management Plan is key for an efficacious project that helps to ensure your device is safe and meets the regulatory requirements.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Developing-an-Effective-Risk-Management-Plan-for-Medical-Devices-504500/MARCH-2018-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar on Step-by-Step Process for Successful Sterility Failure Investigations

    There is no one size fits all investigation for microbial contamination. Microbiological testing covers a wide range of products, processes and environments, therefore representative samples from each of these categories forms the basis of what gets investigated. The role of QC microbiology in the identification and investigation of various results from manufacturing areas and finished product testing is extremely important. When the need for an investigation arises, it is common for a cross functional team to convene involving all levels of management from various departments - quality control chemistry and microbiology, manufacturing, quality assurance, and, facilities and engineering.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Step-by-Step-Process-for-Successful-Sterility-Failure-Investigations-506465/MARCH-2018-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on Medical Device Complaints & CAPA

    This webinar will explain the CAPA process from information gathering through MDR and Recall decision making to final CAPA closing. Post closing effectiveness evaluation is required and will be explained. Preventative Action is often neglected and will be discussed. Post distribution product monitoring including customer surveys will be explained. Integration of manufacturing non conformities with the CAPA program will be discussed. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Medical-Device-Complaints-CAPA-503680/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar on Time Series Analysis Using MS Excel

    Medical device manufacturers must analyze complaints, process data, non-conformances, service records, internal quality audits, etc. This analysis, using appropriate statistical methodology under §820.100 and ISO 13485:2016, 8.4, identifies issues in the quality management system. The result can lead to corrective action and other improvement opportunities. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Time-Series-Analysis-Using-MS-Excel-502148/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar on Applying Human Factors and Usability Engineering Throughout the Medical Device Development Lifecycle

    This session will describe techniques that, when applied appropriately, can greatly impact product safety and usability. Product developers looking to maximize safety, usability, and satisfaction with their products, as well as human factors engineers who want to help developers to accomplish this, will benefit from this course.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Applying-Human-Factors-and-Usability-Engineering-Throughout-the-Medical-Device-Development-Lifecycle-508886/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar on Human Factors Usability Studies Following ISO 62366 and FDA Guidance

    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 https://www.onlinecompliancepanel.com/webinar/Human-Factors-Usability-Studies-Following-ISO-62366-and-FDA-Guidance-504868/JANUARY-2018-ES-TRAININGREGISTRY