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Courses

  • 81 Request Info

    Webinar On Risk Management Using ISO 14971:2007 and EN ISO 14971:2012

    Risk management is essential to device design and required by other standards, such as usability engineering, biocompatibility and electrical safety. The basis is ISO 14971:2007, but many companies don't understand the standard, don't follow the process flow, and consequently don't have an effective implementation. This presentation helps you avoid the common problems and create a compliant system.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/ISO-14971-2007-501829/DECEMBER-2016-ES-TRAININGREGISTRY
  • 82 Request Info

    Webinar On Key Success Factors to reduce your risk of FDA Citations

    Does your company have the symptoms of a sick Quality System? This webinar will help you recognize the symptoms. You will learn about the risks and what you can do about them. Learn from an industry expert how you can improve your Quality Management System.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/RISK-FDA-CITATIONS-501812/OCTOBER-2016-ES-TRAININGREGISTRY
  • 83 Request Info

    Webinar On FDA Regulation of Digital Health - Current Status and Recent Developments

    Why is the FDA focusing on Digital Health? Many medical devices now have the ability to connect to and communicate with other devices or systems. Devices that are already FDA approved or cleared are being updated to add digital features.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/FDA-REGULATION-DIGITAL-HEALTH-501646/AUGUST-2016-ES-TRAININGREGISTRY
  • 84 Request Info

    Webinar On Risk Based Approach for Medical Device Design Control

    This course will explain how to manage a Design Control program that will meet FDA requirements and minimize chances of your medical device being recalled. Such a program will also help to get projects completed on time and within budget. The important and confusing question of when, in a development process, Design Control begins will be answered. The difference between pre-release and post release change control will be explained.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/RISK-BASED-APPROACH-MEDICAL-DEVICE-DESIGN-501511/AUGUST-2016-ES-TRAININGREGISTRY
  • 85 Request Info

    Webinar On Identifying and Addressing Cybersecurity Risks for Medical Devices

    Reports of cybersecurity attacks are appearing more and more frequently in the news affecting e-commerce, retail, the financial industry, the power grid, and in the healthcare setting. With more devices connected as part of the internet of things (IoT), the risks and number of potential threats increases exponentially. Connected medical devices present a unique set of risks due to the element of patient safety and potential for catastrophic outcomes.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/CYBERSECURITY-RISKS-MEDICAL-DEVICES-501617/JULY-2016-ES-TRAININGREGISTRY
  • 86 Request Info

    Webinar On Using Analysis of Variance(ANOVA) - A Practical Approach

    This webinar provides a powerful statistical tool called Analysis of Variance (ANOVA) that you can use to analyze data and improve processes. Because the tool is available in Excel, you don't need to purchase an expensive complicated software package. It is already available to you.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/USING-ANALYSIS-VARIANCE-ANOVA-501564/JULY-2016-ES-TRAININGREGISTRY
  • 87 Request Info

    Webinar On Process Validation - Current Industry Practices and FDA Guidance Document Review

    Process validation is an important subject for the pharmaceutical quality or regulatory professional. Process validation can be difficult and can cause confusion due to different standards, approaches, and process complexities. In this webinar, the basics of process validation will be explored along with current industry practices. The recent draft FDA Guidance Document on process validation will be reviewed and case studies will be presented that will allow the attendee to see practical examples of process validation protocols.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/PROCESS-VALIDATION-FDA-GUIDANCE-501491/JULY-2016-ES-TRAININGREGISTRY
  • 88 Request Info

    Webinar On Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries

    This technical writing training program will offer attendees an understanding of how the reporting process supports products in research, development, and in the marketplace. This virtual session will highlight the mandates for documentation set forth by the regulators, such as the FDA, the ISO, and other governing bodies. The program will train attendees on effectively reviewing and revising documents and assessing your audience, in effect producing effective written correspondence.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/TECHNICAL-WRITING-PHARMACEUTICAL-MEDICAL-BIOTECH-501535/JUNE-2016-ES-TRAININGREGISTRY
  • 89 Request Info

    Webinar On 21 CFR Part 11 - Electronic Record and signature Validation

    This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security. Procedures for controlling electronic signatures and electronic records will be explained.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/21-CFR-PART-11-ELECTRONIC-RECORD-SIGNATURE-VALIDATION-501462/JUNE-2016-ES-TRAININGREGISTRY
  • 90 Request Info

    Two Days Workshop On Statistical Analysis for Process and Product Development

    This course is designed to help scientists and engineers apply statistical methods used to assist decision making in process and product development. Variability must be considered when utilizing data to arrive at conclusions. This course will cover Basic Statistics and Graphical Methods used to summarize data. You will learn how to apply Hypothesis Testing methods to determine whether groups are statistically equivalent or not with respect to key process characteristics such as process averages and variability. Single Registration :- $1,400.00 http://www.onlinecompliancepanel.com/workshop/STATISTICAL-ANALYSIS-800008/APRIL-2016-ES-TRAININGREGISTRY
  • 91 Request Info

    Process Capable Tolerancing® (PCT) Training

    1 Day Who should attend: Designers, Design Engineers and those involved with supplier selection. The statistical concepts behind the process capability index Cpk and its importance to the engineers and designers will be explained in layman's terms. After presenting an introduction to tolerance stack up using the vector method, the Process Capable Tolerancing™ (PCT) methodology for creating components and products that are robust to process variation is presented. The Tolerance Capability Expert™ (TCE) software which facilitates the application of this methodology is demonstrated. The methodology is illustrated through industrial case studies
  • 92 Request Info

    Managing Risks in High-Stakes Projects

    Builds practical skills in using tools & techniques to identify the sources of uncertainty that give rise to risks in high-stakes projects. Also, how to isolate and absorb the uncertainty factors to limit their potential impact. See online description for additional details.