Engineering Management

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  • 1 Request Info

    Effectively Manage Technical, IT, and Engineering Professionals

    Managing technical professionals requires special skills to apply general management principles. o Get results efficiently: plan, delegate, motivate, coach o Communicate; build engaged, high- performing team. o Experiential learning: customized case studies, self-assessments, Action Plan
  • 2 Request Info

    Management/Leadership Power Tools for Engineers

    Engineers become managers because of technical expertise. They need a different skill set. Learn to communicate, plan, motivate, delegate, and coach effectively and efficiently using powerful, proven approaches tailored to your specific situation.
  • 3 Request Info

    Collaboration 4 Project Results

    High energy, interactive 3-day PMBOK-based course for Proj.Mgrs. Teaches processes/ techniques for shaping, energizing, motivating project teams to get faster/better results with Collaboration,“The Tenth Knowledge Area.Bob Moir 404.338.0715
  • 4 Request Info

    Design Inputs Design Outputs Traceability Matrix

    Overview: If your design and manufacturing resources are spending too much time on documentation and not enough time on actual design and manufacturing you as a manager need to be looking for ways to simplify their work. Areas Covered in the Session: Brief introduction to Lean Documents and Lean Configuration. Quality System Regulation, 21 CFR Part 820, and ISO 13485 as these apply to design control documents. Traceability Matrix. Applying lean document and lean configuration principles to the above. Bringing it all together
  • 5 Request Info

    It is not enough to Simply be a Project Manager

    Overview: We manage tasks and activities, and those activities must be performed by people, who must be led. It is not enough to simply be a Project Manager. Why should you Attend: On average it takes ten successful projects to make up for one really bad project. If your projects are finishing late, if your teams turn over faster than a freshman class in college, if your projects are losing money, then you need to take this course.
  • 6 Request Info

    A Risk Based Approach To IT Infrastructure Seminar 2018

    GxP Regulated companies are dependent on validated GxP computerized applications to conduct their day to day operations. These applications are, in turn, depended upon a qualified infrastructure that can be relied upon to provide control and regulatory compliance. The consequences of the IT Infrastructure being out of compliance can result in the failure of an entire site or geographic region being brought to a standstill while the compliance issue is resolved. It can also result in regulatory citations during a regulatory inspection as both the infrastructure be out of compliance and also cause the computerized applications that are dependent on it to be out of compliance.
  • 7 Request Info

    MVP Training: Engineering Management

    MVP Seminars LLC, is a leading nationwide provider of business training seminars at affordable prices, with top-notch providers. Follow-up monitoring program no-charge! Please call 510-558-3495. Largest family run training business in USA.
  • 8 Request Info

    Webinar On Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries

    This technical writing training program will offer attendees an understanding of how the reporting process supports products in research, development, and in the marketplace. This virtual session will highlight the mandates for documentation set forth by the regulators, such as the FDA, the ISO, and other governing bodies. The program will train attendees on effectively reviewing and revising documents and assessing your audience, in effect producing effective written correspondence.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/TECHNICAL-WRITING-PHARMACEUTICAL-MEDICAL-BIOTECH-501535/JUNE-2016-ES-TRAININGREGISTRY
  • 9 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
  • 10 Request Info

    Webinar On Failure Mode and Effects Analysis

    Failure Mode Effects Analysis (FMEA) is a closed loop continuous improvement activity that begins by planning for quality. It identifies what can go wrong with a product or process, the severity and probability of the undesirable event, and existing controls (if any) to prevent or mitigate the problem. It is however not a once-and-done activity because it is updated to reflect actions taken to remove or mitigate failure modes.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/FAILURE-MODE-EFFECTS-ANALYSIS-501614/AUGUST-2016-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On Stability Studies & Estimating Shelf Life

    This webinar discusses the steps to set-up a stability study and analyze the results to estimate the product's shelf life. The use of regression models to model the relationship between the response variable(s) and time are presented. Models useful for describing non-linear degradation over time are also presented. Additionally, methods for handling non-normal response data are also discussed.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/STABILITY-STUDIES-ESTIMATING-SHELF-LIFE-501603/AUGUST-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On How to use Risk Based Process Safety's skills to be in compliance with ICH-Q9 "Quality Risk Management" in the Pharmaceutical Industry

    This webinar will cover the similarities between the second pillar "Knowing the Process" of the Risk Based Process Safety Management and ICH-Q9 "Quality Risk Analysis". This webinar will provide the tools and help to identify the process required information to perform the quality risk by using methodologies in the process hazard analysis (PHA) to determine possible deviation during the process to achieve the good quality of the finished product.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/QUALITY-RISK-MANAGEMENT-PHARMACEUTICAL-INDUSTRY-501651/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Regulatory Document – Site Master File

    This webinar will guide the manufacturer of medicinal products in the preparation of a Site master file (SMF) that is useful to the regulatory authority in planning and conducting GMP inspections.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/SITE-MASTER-FILE-501708/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Learning Design Controls through Review of FDA 483 Observations

    This webinar will provide participants with key knowledge of medical device design controls by analyzing FDA 483 observations and learning what the agency is looking for with respect to each design control element.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/DESIGN-CONTROLS-FDA-483-501773/OCTOBER-2016-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Acceptance Activities in QSR

    Warning Letters from FDA frequently cite Acceptance Activities. In fact, it has been in the top five most frequently cited sections over the past few years. You can avoid a Warning Letter if you understand the regulations and develop processes to implement them. This presentation provides knowledge and tools to help implement an effective system that will withstand an FDA Inspection.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/ACCEPTANCE-ACTIVITIES-QSR-501690/OCTOBER-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Implementation of Document Control Systems

    Regulations mandate effective content control. In an era of continuous flow of information and a regulatory guidance for Knowledge Management (KM) as an enabler of Pharmaceutical Quality System (PQS) Pharmaceutical and Biopharmaceutical firms realize the need to have easy to use Document Control and Management Solutions (DCMS).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/DOCUMENT-CONTROL-SYSTEMS-501811/OCTOBER-2016-ES-TRAININGREGISTRY
  • 17 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
  • 18 Request Info

    Webinar On Overview of the Mexican Labeling Standards and the New Labeling Requirements

    In this 90 minutes session, attendees will learn the Mexican labeling standard as well as and the new requirements regarding the use of Front of Pack icons and the voluntary nutritional quality seal. The regulation has been amended; the most significant change with the new regulations is the mandate to include an FOP nutrition label with information icons on saturated fat, other fat, sugar, sodium, and energy as a percentage of daily nutrients. 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/NEW-MEXICAN-LABELING-REGUIREMENTS-501822/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Conducting a Software Validation of Medical Device to Meet FDA Requirements

    This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation. How software requirements are used in validation will be described. This course is not a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.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/SOFTWARE-VALIDATION-MEDICAL-DEVICE-501884/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Safe Work Practices: OSHA Compliance with Flammable and Combustible liquids

    Flammable materials are substances that can ignite easily and burn rapidly. They can be common materials that are at the most work sites in gas, liquids or solids. In addition, flammable materials may themselves represent a health hazard. This webinar will cover only the flammable and combustible liquids handling and storage. This webinar will cover OSHA and NFPA standards that govern the handling and storage of these liquids. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/SAFE-WORK-PRACTICES-501670/DECEMBER-2016-ES-TRAININGREGISTRY