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  • 1 Request Info

    Certificate in Data Analytics

    The Certificate in Data Analytics program offers users an introduction to data analysis. Learn to use statistics for management and making reliable business decisions with the following courses: Data Analysis for Improving Organizational Performance, Data Analysis in the Real World, Introduction to Data Analysis, Statistical Process Control, Statistics as a Managerial Tool, and Tools of Data Analysis.
  • 2 Request Info

    Webinar On Datafication of HR: Making the Transition from Metrics to Business Analytics

    Leading organizations are using metrics to drive decisions around people. But how can we move from measures to analysis? Oftentimes, HR focused metrics fall short of delivering the types of insight business leaders need to drive business impact. This webinar will provide tools and strategies for using descriptive analytics, diagnostic analytics, and prescriptive analytics in Human Resources in a manner that will initiate better people intelligence. Participants will learn what it takes to make the transition from operational reporting to strategic analytics and impact.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/DATAFICATION-HR-BUSINESS-ANALYTICS-503806/AUGUST-2017-ES-TRAININGREGISTRY
  • 3 Request Info

    Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes 2017

    Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable. One such example is the Medical Device Single Audit Program [MDSAP], where Authorized Organizations would be allowed to carry out a single GMP audit on medical device manufacturing facilities and have it stand to support registrations across the current participating member countries: U.S. Canada, Brazil, Australia and Japan.
  • 4 Request Info

    Online SQL Training Course

    Our SQL Programming course is offered via Web-based training and is available to students across North America, Europe and the Asia-Pacific region. The course consists of about 10 hours of audio/video presentation and about 16 hours of carefully guided hands-on lab exercises.
  • 5 Request Info

    Webinar On Data Visualization and Infographics with Excel

    In this session, you'll learn how to create and enhance the appearance of traditional charts such as bar charts. You'll also learn how to create Sparkline charts (really useful in dashboards), infographic-style charts and how to represent data in a visual way without using the charting features at all. 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/DATA-VISUALIZATION-INFOGRAPHICS-EXCEL-509044/JULY-2017-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On Advanced Auditing Strategies to Detect and Mitigate Data Integrity Risks

    Any successful records management plan will start with a benchmark assessment of your current state followed by a data integrity audit. This training program will teach attendees best practices on how to perform audits for data integrity within their organization. Attendees will also learn how to centralize management and eliminate silos.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/AUDITING-DATA-INTEGRITY-RISKS-509850/JUNE-2017-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On Improving Process Stability and Capability - Tips, Traps and Guidance

    Learn the "What", "Why" and "How" of improving process capability and stability. Topics discussed include: FDA Guidance, pharma and biotech industry experience, pitfalls to avoid, sampling procedures and data quality.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/IMPROVING-PROCESS-STABILITY-CAPABILITY-508219/JUNE-2017-ES-TRAININGREGISTRY
  • 8 Request Info

    ZOS and DB2 Training Courses

    SETC Training’s z/OS and DB2 training courses provide IT professionals with enterprise class mainframe training courses. Our mainframe curriculum covers the full range of topics including z/OS and DB2 administration, configuration, use and development. If you are new to mainframe environments, SETC Training can provide you with a solid introduction to the z/OS operating system, the WebSphere server or the DB2 relational database environment. If are an experienced mainframe professional, we can offer you advanced DB2, z/OS and WebSphere development, administration debugging and troubleshooting training courses. SETC Training also offers an automatic 10% discount, guaranteed dates and free course customization services for groups of 2 people or more.
  • 9 Request Info

    PLSQL Training Courses

    The Oracle PLSQL training courses at SETC Training are based on industry best practices and standards. Every PLSQL training course is based on proper production coding practices in an enterprise database environment. You learn how to build and implement relational databases using the Oracle RDBMS. We offer everything from basic PLSQL syntax to advanced XML and Java integration with the PLSQL language. The PLSQL courses at SETC Training cover cursors, collections, report generation, object oriented programming, indexing, tuning and optimization and much more. SETC Training also offers an automatic 10% discount, guaranteed dates and free course customization services for groups of 2 people or more.
  • 10 Request Info

    Webinar On Dos & Don'ts Related to Information Security and Data Privacy

    This training program will prepare your organization to understand the need for data security, the steps that can be taken to institute or augment your data security policies/procedures, and the implementation of the needed controls. This webinar will introduce attendees to a set of known and respected data security standards that can be employed by your organization to improve your security. Attendees will walk away with ideas to leverage the curriculum with their existing security infrastructure.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/DOs-DOnts-INFORMATION-SECURITY-DATA-PRIVACY-505222/JUNE-2017-ES-TRAININGREGISTRY
  • 11 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
  • 12 Request Info

    Introduction to MEAN Stack Development

    MEAN (MongoDB, Express, AngularJS, and Node.JS) represents a new breed of software platforms that creatively leverage a stack of production-ready technologies centered on JavaScript. This course introduces students to the essential concepts, design principles, idioms, and techniques behind the efficient use of the MEAN JavaScript Technology Stack. Upon completion of this training course, students will have solid understanding of MEANS' value proposition; they will also gain practical experience working with all the components of the MEAN stack. Comprehensive hands on exercises are integrated throughout to reinforce learning and develop real competency.
  • 13 Request Info

    Webinar On Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

    Total Organic Carbon (TOC) is a useful analytical method for cleaning validation studies, including design, qualification and routine monitoring. While there may be some confusion with the industry and regulatory bodies about the use of this analytical technique, it is widely used because of certain benefits. The basis of TOC as an analytical technique will be covered, involving the various technologies currently utilized. Cautions in sampling and analyses will be discussed, including the appropriate use of blank and controls.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/TOC-ANALYSIS-CLEANING-VALIDATION-509928/MAY-2017-ES-TRAININGREGISTRY
  • 14 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
  • 15 Request Info

    Webinar On Medical Device Recalls: a Preventive Strategy

    The secret to preventing medical device recalls is to implement and follow basic practices for specifications and design control, design for process reliability, production validation and design validation using accelerated life tests. This webinar is about controlling safety risk from specification writing to device retirement - control throughout the product's life cycle.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/MEDICAL-DEVICE-RECALLS-509325/APRIL-2017-ES-TRAININGREGISTRY
  • 16 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
  • 17 Request Info

    Webinar On Medical Device Premarket and Post market Cyber security following the new FDA Guidances

    Medical devices, like other computer systems, can be vulnerable to security breaches, potentially impacting the safety and effectiveness of the device. This vulnerability increases as medical devices are increasingly connected to the Internet, hospital networks and to other medical devices. This webinar will describe a program that will minimize risk to the user from cyber attacks.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/MEDICAL-DEVICE-PREMARKET-509863/APRIL-2017-ES-TRAININGREGISTRY
  • 18 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
  • 19 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
  • 20 Request Info

    Webinar On Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration

    Design controls involve the translation of user requirements (aka Voice of the Customer) into specific technical requirements as design inputs. These design inputs then form the basis of the design specification, which becomes the design output. Since design controls requires tracing backwards and forwards in order to link the requirements to their satisfaction, a problem faced by many companies is in having to maintain duplicate information across many controlled documents.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/DESIGN-INPUTS-OUTPUTS-TRACEABILITY-MATRIX-504902/MARCH-2017-ES-TRAININGREGISTRY