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  • 161 Request Info

    Webinar on People Skills for Project Managers

    You may be great at your profession. You may have a spectacular list of achievements. Anyone who is a project manager needs to understand the importance of honing skills that go beyond the technical knowledge to do the job. Therefore if you lack a few essential soft skills, you won't get too far - in your personal life or professionally as a project manager. Like it or not, social skills are essential survival skills. They let you adjust to varying environments. 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/People-Skills-for-Project-Managers-502798/MARCH-2018-ES-TRAININGREGISTRY
  • 162 Request Info

    Webinar on Multi-state Regulation Coordination! Learn How Employers Can Ensure Compliance with Current, New and Proposed State Specific Laws!

    Many companies have challenges keep track and keeping up with all the workplace laws and regulations that impact companies with more than 20 employees when they are in one state. Think of the challenges when the company has locations in multiple states and even across International locations. From staffing, hiring, compensation, background screening, employee leave management, performance, social media, public sector, termination and discrimination are just some of the areas that will impact the risk management in companies and companies should take this seriously. 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/Multi-state-Regulation-Coordination-Learn-How-Employers-Can-Ensure-Compliance-with-Current-New-and-Proposed-State-Specific-Laws-504189/MARCH-2018-ES-TRAININGREGISTRY
  • 163 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
  • 164 Request Info

    Webinar on Global Harmonization with New SDS (Safety Data Sheet) Format

    OSHA has made a significant revision to the HazCom Standard with the new Globally Harmonized Standard (GHS) with a new Safety Data Sheet (SDS) format. This webinar will give participants a comprehensive overview of the new OSHA GHS 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/Global-Harmonization-with-New-SDS-Safety-Data-Sheet-Format-505972/MARCH-2018-ES-TRAININGREGISTRY
  • 165 Request Info

    Webinar on FDA - Streamlining Your Internal Auditing Process

    This webinar will cover creating of a value-added internal auditing program that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485. It will include how to set up and manage the auditing system as well as how to conduct an internal audit and document the results and any nonconformities. It will discuss the value of a good internal auditing program. 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-Streamlining-Your-Internal-Auditing-Process-506001/MARCH-2018-ES-TRAININGREGISTRY
  • 166 Request Info

    Webinar on Process Validation – Principles and Protocols

    This validation training will set forth the regulatory requirements for process validation, and will also include definitions and application of applicable terminology, and hints and recommendations for the more common types of process validation.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/Process-Validation-Principles-and-Protocols-502086/MARCH-2018-ES-TRAININGREGISTRY
  • 167 Request Info

    Webinar on Is Your Vendor Ripping You Off? Fraud Red Flags Corporate Executives Should Recognize

    This training program will primarily focus on analytical and accounting red flags in purchasing schemes, bid rigging, billing schemes, personal purchase schemes, product substitution and all other kinds of corporate fraud. 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/Is-Your-Vendor-Ripping-You-Off-Fraud-Red-Flags-Corporate-Executives-Should-Recognize-503493/MARCH-2018-ES-TRAININGREGISTRY
  • 168 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
  • 169 Request Info

    Webinar on Validation of Complex Cell-Based Potency Methods

    Some cell-based methods are multifaceted. This webinar will address development and validation of complex cell-based methods. It will discuss the selection of the method and the cell line, correlating the method with the pharmaceutical activity, the need for orthogonal methods, and the timeline for method validation. 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/Validation-of-Complex-Cell-Based-Potency-Methods-503812/MARCH-2018-ES-TRAININGREGISTRY
  • 170 Request Info

    Webinar on CAMELS Evaluation and Ratings System plus Examination of CCAR and CLAR

    The webinar will provide an in depth understanding of the CAMELS methodology and evaluation process in order to address any deficiencies that may exist before a CAMELS evaluation is conducted. Attendees will gain an in depth understanding of the FRB's approach to its CCAR and CLAR evaluation considerations, processes and ratings. 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/CAMELS-Evaluation-and-Ratings-System-plus-Examination-of-CCAR-and-CLAR-503046/MARCH-2018-ES-TRAININGREGISTRY
  • 171 Request Info

    Webinar on EDD: What are the Auditors Looking for?

    This webinar will explain the concept of Enhanced Due Diligence (EDD), including EDD time tables and the checklist. Attendees will learn how to conduct Enhanced Due Diligence (EDD) that will satisfy the auditors/examiners/regulators look for with respect to EDD so you are not wasting your time and resources and still keeping the auditors/examiners/regulators happy. Also, by conducting proper EDD reviews your institution can confirm that all Customer Due Diligence (CDD) information is up to date as well as accurate and ensures that it is not being taken advantage of by individuals/entities that would try to exploit it for nefarious purposes. 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/EDD-What-are-the-Auditors-Looking-for-508405/MARCH-2018-ES-TRAININGREGISTRY
  • 172 Request Info

    Webinar on EU GMP Annex 1 - What's New for Sterile Product Manufacturing?

    A major revision is taking place with the European regulations covering the manufacture and distribution of sterile products. This is the first major update in 20 years, with the new draft text bringing in many changes, several of which will be far reaching. 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/EU-GMP-Annex-1-What-s-New-for-Sterile-Product-Manufacturing-507684/MARCH-2018-ES-TRAININGREGISTRY
  • 173 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
  • 174 Request Info

    Webinar on AML for International Correspondent Banking

    This webinar will address the many risk issues related to AML compliance and how the Bank can address these risks. 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/AML-for-International-Correspondent-Banking-504102/MARCH-2018-ES-TRAININGREGISTRY
  • 175 Request Info

    Webinar on Appraisal Program Guidance

    There is no "one size fits all" when it comes to a regulatory compliant appraisal program, but good appraisal programs share some common traits. This webinar examines alternatives and best practices for appraisal programs, all of which balance production enhancement and risk mitigation. Regulatory compliance starts with a reasoned and comprehensive appraisal program, which flows through to policy and procedures into every day practice in the bank. 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/Appraisal-Program-Guidance-507324/MARCH-2018-ES-TRAININGREGISTRY
  • 176 Request Info

    Webinar on A Regulatory Perspective: FDA's New Guidance's Deciding When to Submit a 510(k) for Device & Software Changes

    Control of medical device changes and a current 510(k) are big issues in recent FDA studies. Companies are held fully responsible for deciding when a new 510(k) filing is warranted. Often this is a difficult decision process. Effective change control and the power of current risk management tools must be a major part of such an analysis. 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/A-Regulatory-Perspective-FDA-s-New-Guidance-s-Deciding-When-to-Submit-a-510-k-for-Device-Software-Changes-508234/MARCH-2018-ES-TRAININGREGISTRY
  • 177 Request Info

    Webinar on Stability Studies and Estimating Shelf Life with Regression Models

    Manufacturers of foods, drugs, consumer goods, and other products must determine the shelf life of their products so that customers know when the product can be expected to perform as intended. Many approaches are available to quantify the "shelf life" and the method(s) chosen often depend on the testing time available. 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/Stability-Studies-and-Estimating-Shelf-Life-with-Regression-Models-506813/MARCH-2018-ES-TRAININGREGISTRY
  • 178 Request Info

    Webinar on HR Metrics & Analytics 2018: Update on Strategic Planning, Application Activities and Operational Impact

    The purposes of an organization's human resources are to add value, make the organization more competitive, and help the organization achieve its business objectives. The purposes of HR metrics are to help communicate the value added, demonstrate the contribution of human capital, and measure employment related risks. Thus, to become a strategic partner, HR professionals need to speak the language of business. Inherent in that language is the lexicon of business measurements and metrics? Including HR metrics. 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/HR-Metrics-Analytics-2018-Update-on-Strategic-Planning-Application-Activities-and-Operational-Impact-502859/MARCH-2018-ES-TRAININGREGISTRY
  • 179 Request Info

    Webinar on Biosimilars from Development to Registration

    The European Union (EU) currently has around a decade of experience with biosimilars. The first wave of biosimilars comprised simple biologics, such as somatropin, erythropoietin and filgrastim. The European Commission (EC) granted marketing authorization for 14 biosimilars between April 2006 and June 2010. The approval of the first monoclonal antibody (mAb) biosimilar in 2013 - Inflectra/Remsima from then Celltrion and Hospira - marked the beginning of the second wave of approvals and the first of the more complex biosimilars. 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/Biosimilars-from-Development-to-Registration-504679/MARCH-2018-ES-TRAININGREGISTRY
  • 180 Request Info

    Webinar on Root Cause Analysis (RCA) in the Laboratory - Addressing Non-Conformances

    This RCA webinar will define a specific set of steps and associated tools that you can use to determine the primary cause of non-conformance in your laboratory. You will learn to determine what happened, why it happened and how to reduce the likelihood of that non-conformance happening again. 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/Root-Cause-Analysis-RCA-in-the-Laboratory-Addressing-Non-Conformances-504547/MARCH-2018-ES-TRAININGREGISTRY