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  • 1 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
  • 2 Request Info

    Database Fundamentals

    +Database Systems and Relational Databases +Management of Relational Database Data
  • 3 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.
  • 4 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.
  • 5 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
  • 6 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
  • 7 Request Info

    Power BI: Driving Results with Your Data

    Overview In today's fast-paced, high-tech, competitive business environment, analytics, data visualization and Business Intelligence (BI) are the hot topics many firms and professional recruiters seek.
  • 8 Request Info

    Compliance with 21 CFR Part 11, SaaS-Cloud, EU GDPR [Data Integrity]

    Overview: This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud hosted applications. It explains how to write a Data Privacy Statement for compliance with EU General Data Protection Regulation (GDPR). What the regulations mean is described for all four primary compliance areas: SOPs, software features, infrastructure qualification, and validation. It gets you on the right track for using electronic records and signatures to greatly increase productivity and ensure compliance.
  • 9 Request Info

    Implementation and Management of GMP Data Integrity

    Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition applies to data recorded in electronic and paper formats or a hybrid of both. To assure the quality of raw materials, in process materials and finished goods,laboratory data integrity is assuming greater importance in current Good Manufacturing Practices (CGMP) for US Food and Drug Administration (FDA)-regulated industry. Data integrity and security infractions are not only 21 Code of Federal Regulations (CFR) Part 11 issues but also severe CGMP violations.
  • 10 Request Info

    Project Management for Non-Project Managers

    Overview: This webinar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject. Why should you Attend: It is not possible to present a complete treatment of project management in the span of 60-90 minutes. It is however possible to focus in on those most critical project management aspects that are critical to the success of any project. Without basic tools, it is not possible to effectively manage a project to the pre-determined end-date without turmoil and chaos.
  • 11 Request Info

    Equipment Validation, Tracking, Calibration and Preventive Maintenance

    Overview: FDA and EU regulations require that firms have a program for the calibration and maintenance of test and measurement equipment. The program must include: intervals, scheduling, specific procedures, limits of accuracy/precision, and remedial action in the event that the equipment does not meet established requirements. Prior to use, however, this equipment must be validated to make sure it produces product that meets its specifications. There are ways, though, to validate equipment already in use.
  • 12 Request Info

    Webinar on Sampling Plans for Process Validation and Production Lot Acceptance

    This webinar covers Acceptance Sampling plans for process validation and production lot acceptance. Sampling plans for attribute data are the primary focus although variable acceptance sampling plans are presented as well. The binomial distribution and its use in developing Operating Characteristic (OC) Curves is discussed. The key inputs to determining sampling plans (AQL, RQL, Consumer's and Producer's Risks) are described in detail.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/ACCEPTANCE-SAMPLING-PLANS-501157/FEB-2016-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar on Computer System Validation and User Acceptance Testing

    This course provides an understanding of computerized system validation process and the important role of Users in that process by way of User Acceptance Testing.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/COMPUTER-VALIDATION-SYSTEM-501285/MARCH-2016-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Working with Data Models in Excel 2013+

    Many Excel data crunchers mourned the loss of easy access to PowerPivot as Excel 2013 was released. However, one of its most powerful features, the ability to analyze multiple related datasets, is now included in most versions of Excel as part of the data model.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/WORKING-DATA-MODELS-EXCEL-2013-501673/AUGUST-2016-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Blockchain for Risk Management /Data Security: Emerging Technological Approach for KYC and Secure Transactions

    A Blockchain is a transaction database shared by all nodes participating in a system based on the Bitcoin protocol. This course describes, what Blockchain is and its financial applications to creating secure KYC and payment data sets. This course also explains a Blockchain concept where the Blockchain itself is a shared single source of truth.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/BLOCKCHAIN-RISK-MANAGEMENT-DATA-SECURITY-501662/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Data Protection Act and the ISO27000

    The training will provide critical understanding of important IT security issues for all types of organizations that feel they do not fall under specific IT regulatory frameworks. Additionally, the training will enable IT and related staff at all unregulated organizations to better understand data security.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-PROTECTION-ACT-ISO27000-501626/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On How to Conduct an Effective Annual Product Quality Review

    This webinar will give a brief overview of the general procedure for the preparation and documentation of the Annual Product Quality Review and also focuses on the regulations and the regulatory requirements as per US and Europe. It will also discuss the comparative evaluation about similarities and differences of requirements associated with the manufacturing of the drug product in different countries.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-ANNUAL-PRODUCT-QUALITY-REVIEW-501733/OCTOBER-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On Getting the most from your data with Access Queries

    Microsoft Access is a very powerful database management tool, but it is not very intuitive. In this webinar, you will learn how to take your raw data and create meaningful reports that will help you get the most of your data using this software. As a business owner or manager, you have mounds and mounds of raw data transactions, and it is a monumental task to make any sense out of that 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/DATA-ACCESS-QUERIES-501758/OCTOBER-2016-ES-TRAININGREGISTRY
  • 19 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
  • 20 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