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  • 41 Request Info

    Webinar On Understanding and Implementing USP 1058 - Analytical Instrument Qualification

    This webinar is designed to provide both a regulatory compliant and practical overview of equipment / instrument qualification, including requirements associated with instrumental system validation.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/USP-1058-ANALYTICAL-INSTRUMENT-501960/DECEMBER-2016-ES-TRAININGREGISTRY
  • 42 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.
  • 43 Request Info

    Webinar On Train the Trainer: Key Tips for Engaging Adult Learners

    Adult learning is defined as ‘the entire range of formal, non-formal and informal learning activities which are undertaken by adults after a break since leaving initial education and training, and which results in the acquisition of new knowledge and skills’. In order for adults to acquire new knowledge and skills, we must deliver training to meet their learning needs. In this course, you will learn about the theories and methods to engage in Adult Learner.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/KEY-TIPS-ENGAGING-ADULT-LEARNERS-501938/DECEMBER-2016-ES-TRAININGREGISTRY
  • 44 Request Info

    Webinar On Stability Testing for Dietary Supplements

    The purpose is to present recommendation for supporting the voluntary shelf-life (expiration) dating claims of dietary supplements. The purpose of stability testing is to provide evidence on how the quality of formulation varies with time under the influence of a variety of environmental factors. Stability testing permits the establishment of recommended storage conditions and shelf lives.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/STABILITY-TESTING-DIETARY-SUPPLEMENTS-501914/DECEMBER-2016-ES-TRAININGREGISTRY
  • 45 Request Info

    Webinar On Device Master Record - Can DMR show the way to comply with QSR?

    Device Master Record (DMR) is the output of design controls and the source document for every medical device. An accurate, complete DMR gives the 'recipe' for making a medical device. From the smallest component or ingredient and simplest operation or step to the finished medical device including labels, labeling, primary, secondary and beyond packaging to installation, servicing and maintenance instructions, the DMR has everything including the exact format and content of a medical device's device history record (DHR/batch record).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/DEVICE-MASTER-RECORD-501904/DECEMBER-2016-ES-TRAININGREGISTRY
  • 46 Request Info

    Webinar On 21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

    All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. Medical device manufacturing plants, required to follow 21 CFR Part 820, have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOPs, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.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/21-CFR-PART-820-QUALITY-SYSTEM-501907/DECEMBER-2016-ES-TRAININGREGISTRY
  • 47 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
  • 48 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
  • 49 Request Info

    Webinar On SMED - Single Minute Exchange of Die (reduced changeover)

    (SMED) is a methodology that was created by Shigeo Shingo in the Toyota press room to reduce the time needed to setup and changeover the huge stamping presses. The goal is first to reduce setup times by 50% and ultimately to less than 10 minutes.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/SMED-SINGLE-MINUTE-EXCHANGE-DIE-501874/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 50 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
  • 51 Request Info

    Worhshop On Design of Experiments for Process/Product Optimization

    This course is designed to help scientists and engineers plan and conduct experiments and analyze the data to develop predictive models used to optimize processes and products and solve complex problems. Design of Experiments (DOE) is an extremely efficient method to understand which variables (and interactions) affect key outcomes and allows the development of mathematical models used to optimize process and product performance.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/Design-of-Experiments-for-Process-Product-Optimization-800009/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 52 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
  • 53 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
  • 54 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
  • 55 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
  • 56 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
  • 57 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
  • 58 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
  • 59 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
  • 60 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