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  • 21 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.
  • 22 Request Info

    Project Management for Non-Project Managers 2018

    This Project management training will provide you with a solid foundation for managing that first project or to simply sharpen existing project management skills, It is not just important to learn about project management - project management has its own body of knowledge, Also The webinar is designed to build a working understanding of the subject and for a quick start-up for those unanticipated project management assignments.
  • 23 Request Info

    Overview of Construction Claims & Disputes

    Overview In this webinar expert speaker's James Zack will help you to identify several types of owner claims against contractors and the elements of the burden of proof required of all claimants. The basic requirements concerning damages are covered. The webinar will conclude with an outline of various dispute resolution methodologies.
  • 24 Request Info

    6-Hour Virtual Seminar on GxP/GMP and its Consequences for Quality Management

    GxP/GMP regulations are required to be used in regulated industries such as food, pharmaceutical, medical devices, and cosmetics. GMP regulations describe required quality management system for production and testing of products in these regulated industries. The purpose of the GMP regulations is to ensure that a product is safe and meets its intended use. Quality management system ensures that a product is safe and meets its intended use. Quality management system has four main components: quality planning, quality assurance, quality control, and quality improvement.
  • 25 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.
  • 26 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.
  • 27 Request Info

    Engineering Seminars

    Stay current on existing laws and recent legislation that are influencing the engineering industry. Choose from a variety of seminar topics. Continuing education credits can be obtained where applicable.
  • 28 Request Info

    Engineering Teleconferences

    Stay current on existing laws and recent legislation that are influencing the engineering industry. Choose from a variety of seminar topics. Continuing education credits can be obtained where applicable.
  • 29 Request Info

    MVP Training: Plant Operation & Maintenance

    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.
  • 30 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.
  • 31 Request Info

    MVP Training: Writing Skills For Engineers

    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.
  • 32 Request Info

    Two Days Workshop On Statistical Analysis for Process and Product Development

    This course is designed to help scientists and engineers apply statistical methods used to assist decision making in process and product development. Variability must be considered when utilizing data to arrive at conclusions. This course will cover Basic Statistics and Graphical Methods used to summarize data. You will learn how to apply Hypothesis Testing methods to determine whether groups are statistically equivalent or not with respect to key process characteristics such as process averages and variability. Single Registration :- $1,400.00 http://www.onlinecompliancepanel.com/workshop/STATISTICAL-ANALYSIS-800008/APRIL-2016-ES-TRAININGREGISTRY
  • 33 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
  • 34 Request Info

    Webinar OGMPs for OTC and Cosmetic Products - US and Global Requirementsn

    The cosmetic good manufacturing practice is a set of manufacturing guidelines to ensure the safety and quality of cosmetic products. OTC drug manufacturers, labelers, packagers and holders must comply with good manufacturing practices.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/GMPS-OTC-COSMETIC-PRODUCTS-501385/MAY-2016-ES-TRAININGREGISTRY
  • 35 Request Info

    Webinar On BSA: Marijuana Businesses, Virtual Currency and Model Validation

    This session will offer insights into the application of BSA Requirements on the burgeoning business of medical and recreational marijuana and the silent but effective virtual currency markets and uses, while discussing ways to validate BSA models and applications in monitoring and alerting an institution to potential Money Laundering and other related threats.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/BSA-MARIJUANA-BUSINESSES-CURRENCY-VALIDATION-501485/MAY-2016-ES-TRAININGREGISTRY
  • 36 Request Info

    Webinar On 21 CFR Part 11 - Electronic Record and signature Validation

    This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security. Procedures for controlling electronic signatures and electronic records will be explained.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/21-CFR-PART-11-ELECTRONIC-RECORD-SIGNATURE-VALIDATION-501462/JUNE-2016-ES-TRAININGREGISTRY
  • 37 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
  • 38 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
  • 39 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
  • 40 Request Info

    Webinar On Understanding and Implementing an Effective Laboratory Quality Management System to comply with ISO/IEC 17025

    This training program on implementing an effective laboratory quality management will focus on ISO/IEC 17025 requirements. Attendees will learn how to develop and maintain a quality management system to ensure compliance with the international laboratory accreditation standard.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/EFFECTIVE-LABORATORY-QUALITY-MANAGEMENT-SYSTEM-501579/JULY-2016-ES-TRAININGREGISTRY