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  • 1 Request Info

    Filemaker Fundamentals

    In this FileMaker training, you will complete hands-on exercises to master basic skills as well as learn essential concepts to take your expertise to the next level. See our website for locations and schedule.
  • 2 Request Info

    MySQL Fundamentals

    MySQL training will take you from novice to expert in two information-packed days. In this hands-on workshop, our experienced instructor will introduce you to the MySQL Server environment and database administration. See our website for locations and schedule.
  • 3 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.
  • 4 Request Info

    Fundamentals of Crystal Reports 2011

    +Getting Started with Crystal Reports 2011
  • 5 Request Info

    Crystal Reports XI: Report Writing Basics

    +Crystal Reports XI: Report Writing Basics +Managing Data and Distributing Reports with Crystal Reports XI
  • 6 Request Info

    Mongo DB

    +MongoDB: Indexing, Replication, and Security
  • 7 Request Info

    RavenDB Fundamentals

    +RavenDB Overview +RavenDB Integration
  • 8 Request Info

    Big Data Fundamentals

    +The Big Data Technology Wave +Big Data Opportunities and Challenges
  • 9 Request Info

    Apache Hadoop and MapReduce Essentials

    +MapReduce Essentials +Apache Hadoop
  • 10 Request Info

    MySQL Essentials

    +MySQL: Database Concepts, Design, and Installation +MySQL: Querying Data Using the SELECT Statement +MySQL: Using the Data Manipulation and Definition Statements +MySQL: General Syntax, Advanced Queries, and Stored Programs +MySQL: Advanced Routines, Optimization, and DCL +MySQL: Storage Engines, Advanced Indexing, and Maintenance +MySQL: Administration, Transactions, Optimization, Scaling, Backup, and Recovery +MySQL: Performance Monitoring, Database Health and Integrity, and Security
  • 11 Request Info

    Database Design Fundamentals

    +Database Systems and Relational Databases +Management of Relational Database Data +Introduction to Designing a Relational Database +The Logical and Physical Database Design Methodologies
  • 12 Request Info

    Database Fundamentals

    +Database Systems and Relational Databases +Management of Relational Database Data
  • 13 Request Info

    Data Science Fundamentals in R

    +Fundamental Methods for Data Science in R +Machine Learning Examples for Data Science in R
  • 14 Request Info

    Data Visualization: Essentials

    Data Visualization: Essentials
  • 15 Request Info

    CAPA Training and Causes of Warning Letters

    Overview: A timely, well documented, Corrective / Preventive Action program validates a quality system that is not only capable of identifying potential problems but also effectively correcting problems when incidents do occur and as part of the Continuous Quality Improvement program, correcting potential problems prior to occurrence. Adequate incident tracking is the primary foundational element for an effective CAPA system. Why should you Attend: A vast majority of the current industry deficiencies which have led to isolated 483s, Warning Letters and Consent Decrees are the result of deficient technical documentation and effective means of assessing various elements of CAPA expectations for products produced and distributed under the FDA regulations.
  • 16 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.
  • 17 Request Info

    What is Data Integrity Issues-Types of Data Integrity Issues 2018

    Defined by the Medicines and Healthcare Products Regulatory Agency (MHRA) as "the extent which all data are complete, consistent and accurate throughout the data lifecycle", data integrity is increasingly the focus of regulatory agencies round the world. Companies must now ensure that they are appropriately addressing data integrity and data governance. This includes organizational, procedural and technical controls that must be considered as part of an overarching data governance system. In addition, the effort and resources committed to data integrity must be commensurate with the role it plays in assuring product quality. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901378SEMINAR?trainingregistry-February-2018-SEO
  • 18 Request Info

    Supplier Management Solutions | Medical Device Manufacturers

    Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. How well do you understand the requirements for supplier management? Could you pass a regulatory audit or inspection without any issues? Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901480SEMINAR?trainingregistry-March-2018-SEO
  • 19 Request Info

    A Risk Based Approach To Data Integrity 2018

    The impact of Data Integrity issues on a regulated company can be significant: it can result in recalls of products, warning or untitled letters, import alerts, injunctions, seizures, legal action, etc. These regulatory actions can have significant financial impact to the company. However, and most importantly, data integrity issues can lead to potential patient harm!! Defined by the Medicines and Healthcare Products Regulatory Agency (MHRA) as "the extent which all data are complete, consistent and accurate throughout the data lifecycle", data integrity is increasingly the focus of regulatory agencies round the world. Companies must now ensure that they are appropriately addressing data integrity and data governance. Click to Continue Reading: https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901381SEMINAR?trainingregistry-April-2018-SEO
  • 20 Request Info

    Legal Writing Skills that Result in Effective Regulatory Submissions

    It is essential that professionals in the pharmaceutical and medical device companies clearly understand and effectively employ legal writing techniques to frame persuasive argument when negotiating with FDA. The success or failure of many new drugs, biologic or medical device projects hinges on presenting essential information in a persuasive manner. Do you use these legal drafting skills when preparing quality and regulatory documents?