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  • 1 Request Info

    Webinar on Third Party Risk Management Information Security Process

    Learn about the GDPR's impact on companies that do business with EU citizens and how third party relationships can be managed proactively to address new and emerging 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/How-to-Tackle-Vendor-Risk-Hazards-A-Risk-Based-Management-Approach-to-Third-Party-Data-Security-Risk-and-Compliance-505739/AUGUST-2018-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on Good Documentation Practices to Support FDA Computer System Validation and Compliance

    Learn how to create and maintain good documentation that meets FDA computer system validation and compliance standard. 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/Good-Documentation-Practices-to-Support-FDA-Computer-System-Validation-and-Compliance-504252/JUNE-2018-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on Managing IT and Cyber Asset Management

    This webinar will guide you on how to establish, implement, maintain and improve an asset management system that manages the lifecycle of assets in the organization. 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/Managing-IT-and-Cyber-Asset-Management-508897/JUNE-2018-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on FDA's Quality Metrics Program and Scorecards: Critical Success Parameters

    The speaker Joy McElroy will discuss the role of quality metrics program and scorecards within a company's KPI 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-s-Quality-Metrics-Program-and-Scorecards-Critical-Success-Parameters-502152/MAY-2018-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar on EU GDPR Deadline is Just around the Corner: Understanding Compliance for Clinical Trials for Life Sciences Companies

    Join this webinar to be better prepared to comply with new regulation, as well as understand the terms and definitions used in GDPR relevant to clinical trials. 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-GDPR-Deadline-is-Just-around-the-Corner-Understanding-Compliance-for-Clinical-Trials-for-Life-Sciences-Companies-503375/MAY-2018-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar on The Final Countdown to GDPR Compliance Deadline

    Join us for this webinar to accelerate your GDPR readiness, improve your risk management strategies and help you fulfill GDPR obligations. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/Final-Countdown-to-GDPR-Is-Your-Business-Compliant-for-the-May-25th-Deadline-503290/APRIL-2018-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar on General Data Protection Regulation (GDPR) Compliance for Clinical Trials

    Attend this webinar to know how to be prepared to comply with the new regulation and understand the key principles used in GDPR relevant to clinical trials 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/General-Data-Protection-Regulation-GDPR-Compliance-for-Clinical-Trials-504021/APRIL-2018-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On Solving Statistical Mysteries - What Does the FDA Want?

    This webinar provides an overview of what it appears the FDA is looking for in the use statistics by taking illustrative examples from warning letters and industry experiences and approaches that have worked in a variety of situations.Use of statistics has been part of the FDA's guidance and regulations for many years. Use of statistical tools is an integral part of the Jan 2011 FDA Process Validation Guidance. It can be argued that the FDA is looking for the pharma and biotech industries to make even greater use of statistical thinking and methods. Even with this long history, the use of statistics seems to be a source of uncertainty and anxiety for many.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/SOLVING-STATISTICAL-MYSTERIES-506995/MAY-2017-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Failure Mode and Effect Analysis (FMEA) – Risk Analysis and Management

    Failure Mode and Effects Analysis (FMEA) is a systematic method for preventing failure through the discovery and mitigation of potential failure modes and their cause mechanisms. Actions are developed in a team environment and address each high: severity, occurrence or detection ranking indicated by the analysis. Completed FMEA actions result in improved product performance, reduced warranty and increased product quality.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/FMEA-RISK-ANALYSIS-MANAGEMENT-508377/APRIL-2017-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On Top 10 Ways to Get Sued From Employee Investigation

    Can you investigate without getting sued? Maybe, but isn't it better to first try to make sure there's no basis for a suit to begin with? Making the right decision often turns on the quality of the investigation and how it was conducted because a flawed investigation can expose the employer to a significant and costly legal contest.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/TOP-10-WAYS-SUED-EMPLOYEE-INVESTIGATION-509232/APRIL-2017-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On How to Write an Effective Compliance Investigation Report

    This presentation gives attendees a blueprint for drafting a compliance investigation report that can be applied to varying circumstances. Mr. Anstine will go through each component of the investigation report and provide strategies and tips for drafting. To illustrate how to draft each component of the report, Mr. Anstine will walk attendees through a sample fact pattern of an allegation of non-compliance that needs to be investigated.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/EFFECTIVE-COMPLIANCE-INVESTIGATION-509374/MARCH-2017-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On Data Analysis in QSR

    Data analysis is one of the most powerful improvement tools because it can lead to cost reductions and preventive action. To use these techniques you need to know both the regulatory requirements and the analysis framework. This presentation provides that essential information.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/DATA-ANALYSIS-QSR-507590/MARCH-2017-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Microsoft Excel Data Validation Tools - Keep out Bad Data from the Start, Simplify Data Entry and Ensure Accuracy with this Powerful Featur

    With Excel's data validation tools, you can control how users input data into workbooks and ensure data is entered consistently and accurately. You can control dates, times, and the length of the data they enter, or simply provide a list of acceptable choices to eliminate any possible mistakes. Using Excel's data validation tools you can also control data entry by formulas, provide dropdown lists that eliminate time-consuming and error-prone typing mistakes, control numeric data based on date and time constraints, and identify unwanted data by applying data validation rules on existing data.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/MICROSOFT-EXCEL-DATA-VALIDATION-TOOLS-503086/MARCH-2017-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Data Analytics - Finding the Trends

    Learn the best practices for managing your Big Data Analytics Program - acquiring, organizing, interpreting and summarizing data. Discover the software tools available for data analytics. Receive valuable references to help you analyze and select analytics software. Review the two dimensions of analysis - receive an exhaustive chart of analytic methods and the purpose of each.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/DATA-ANALYTICS-508621/MARCH-2017-ES-TRAININGREGISTRY
  • 15 Request Info

    Two Days Workshop On Quality Management Systems that Comply with ISO13485:2016

    Quality Management Systems that Comply with ISO13485:2016" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.Price:$1400.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/workshop/Quality-Management-Systems-that-Comply-with-ISO13485-2016-800016/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Challenges for Data Collection in Clinical Trials for Low-Cost Wearable Health Monitors

    Activity monitors, smart watches, patches are just some examples of wearable monitors. Health care is full of them, sleep monitors, EKGs, radiation exposure devices, and respirator devices to name a few. With more and more of these devices becoming common place, it's inevitable that researchers will want to mine this data.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/CLINICAL-TRIALS-LOW-COST-WEARABLE-HEALTH-MONITORS-501882/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 17 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
  • 18 Request Info

    Webinar On Getting Results with Crystal Reports

    Crystal Reports is a very powerful tool that can allow you to take many different types of data and combine that data into great reports. However, it requires a little training so you can use it properly and efficiently and to its maximum potential. In this webinar, you will learn how to take your raw data and create meaningful reports using the powerful SAP Crystal Reports software.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/GETTING-RESULTS-CRYSTAL-REPORTS-501759/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 19 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
  • 20 Request Info

    Webinar On How to Use Big Data for AML/AB&C Compliance and Risk Mitigation

    This webinar discusses how Big Data is used for AML compliance review. The instructor will explain how an unstructured data becomes structured and is subjected to data quality review, sampling and subsequent forensic analysis. The instructor will share how this analysis influences strategic decision in terms of risk mitigation and AML Program enhancement.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/BIG-DATA-AML-AB-C-COMPLIANCE-RISK-MITIGATION-501688/OCTOBER-2016-ES-TRAININGREGISTRY