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  • 21 Request Info

    Webinar On Strategic Planning via Hoshin Kanri: Involve your Entire Organization in Achieving Breakthrough Objectives

    This online course provides an overview of strategic planning and a proven method for executing on your goals. Hoshin Kanri (also known as Hoshini Planning, strategy deployment or policy deployment) is a method for involving your entire organization in delivering a combination of breakthrough performance and daily management.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/STRATEGIC-PLANNING-HOSHIN-KANRI--502431/MAY-2017-ES-TRAININGREGISTRY
  • 22 Request Info

    Webinar On Employee Fraud Detection and Prevention

    This fraud training program will focus on understanding the fraud problem and what propels employees to commit fraud. The course will also offer essential fraud detection tools and techniques and highlight best practices for developing and implementing anti-fraud controls. The ultimate goal of all of this, of course, is to lay the groundwork for pinpointing and then remediating internal control deficiencies that provide the opportunities for dishonest employees to engage in fraudulent activity.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/EMPLOYEE-FRAUD-DETECTION-PREVENTION-507384/MAY-2017-ES-TRAININGREGISTRY
  • 23 Request Info

    Webinar On BSA/AML Automated Systems Validation: Validation Insights

    This webinar will discuss the need for the validation process, the expectations of that process and how to address and identify areas of concern when validating the AML process, and the steps to follow and how to deal with it when it doesn't work. Government requirements continue to expand and those requirements continue to place increasing stresses on people and systems. Making sure it works is not only a top priority for compliance but to justify the costs and resources expended. Validation addresses much if not all of those concerns.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/BSA-AML-AUTOMATED-SYSTEMS-VALIDATION-508766/MAY-2017-ES-TRAININGREGISTRY
  • 24 Request Info

    Webinar On Steps to HIPAA Compliance and Ransomware Prevention

    This webinar will explain what the highest risk factors for being sued for wrongful disclosures of PHI are, and the manner in which patients are now using state laws to sue for wrongful disclosures. He will also delve into specific information about multiple incidents, which will help practices and businesses understand what they did wrong that led to a HIPAA risk of ransomware.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/HIPAA-COMPLIANCE-RANSOMWARE-502761/APRIL-2017-ES-TRAININGREGISTRY
  • 25 Request Info

    Webinar On How to Buy COTS Software, Audit Vendors and Validate the Software

    This presentation will focus on instructing attendees on best practices for buying COTS (Commercial Off-The-Shelf) software and evaluating software vendor(s). Presentation will highlight essential data and systems subject to Part 11 & Annex 11 (ERES - Electronic Records and Electronic Signatures) compliance while listing requirements for IT infrastructure, Laboratories, Manufacturing/ Operations, R&D, Regulatory and other GxP relevant areas of an FDA regulated manufacturer. 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/COTS-SOFTWARE-AUDIT-VENDORS-505707/MARCH-2017-ES-TRAININGREGISTRY
  • 26 Request Info

    Webinar On How will Artificial Intelligence (AI) Affect Healthcare?

    I is moving into Healthcare rapidly. There are many models that AI will engage. This topic will cover the new field of AI, its capabilities and how it will impact all aspects of the Healthcare from Supply Chain, to Population Health to direct consumer/patient engagement.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/ARTIFICAL-INTELLIGENCE-AFFECT-HEALTHCARE-505512/MARCH-2017-ES-TRAININGREGISTRY
  • 27 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-POST-MARKET-CYBER-SECURITY-509863/MARCH-2017-ES-TRAININGREGISTRY
  • 28 Request Info

    Balancing Customer Satisfaction With Security Issues

    Overview: Financial institutions have long been the payments engines for their customers. However, with heightened competition and the advent of new non-bank entries into the marketplace, financial institutions have been playing more defense than offense. Why should you Attend: This webinar is designed for professionals in every bank and credit union area to develop and maintain payments as the core business practice for their customers. Every transaction includes a payment of some sort and the banking industry owns the settlement process, for now. Areas Covered in the Session: S.W.O.T Strengths that banks should exploit Weaknesses that banks should shore up Opportunities for banks to take advantage of Threats that banks cannot ignore Who Will Benefit: Payments Professionals Operations Managers Financial Officers Risk Officers Internal Auditors
  • 29 Request Info

    Webinar On 21 CFR Part 11 compliance for Electronic Medical Records

    This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical 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-11-ELECTRONIC-MEDICAL-RECORDS-502044/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 30 Request Info

    Webinar On How to Conduct a Human Factors Validation Test Following ISO62366 and the FDA Guidance

    Validation testing aims to show that a device can be used by the intended users without serious use errors or problems, for the intended uses and under the expected use conditions. This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/ usability validation test. HF/U validation is very different from device validation.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/HUMAN-FACTORS-VALIDATION-ISO62366-FDA-502041/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 31 Request Info

    Webinar On FDA Warning Letter - Consent Decree Software Validation

    This training on FDA software validation related warning letters will discuss what to do to avoid additional software related compliance issues along with the response steps where the citations directly or indirectly include automated system.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-WARNING-LETTER-501955/DECEMBER-2016-ES-TRAININGREGISTRY
  • 32 Request Info

    Webinar On Software FMEA for Medical Devices

    Software related device recalls are steadily going up for the last 10 years. The biggest reason is that missing and vague requirements in software specifications are responsible for at least 50% failures. Therefore risks are inherent in software design and development, even after so much attention paid to the design control process.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/FMEA-MEDICAL-DEVICES-501919/DECEMBER-2016-ES-TRAININGREGISTRY
  • 33 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
  • 34 Request Info

    Webinar On Clinical System Data Management Validation

    Have you validated your clinical data base? Do you have the proper documentation in the event of a regulatory inspection? In this course we will cover considerations and requirements for validation of clinical data management systems. We will discuss the challenges and strategies of risk based validation and review 21 CFR Part 11 expectations. We will discuss the importance of a change control process.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-DATA-MANAGEMENET-501926/DECEMBER-2016-ES-TRAININGREGISTRY
  • 35 Request Info

    Webinar On Conducting a Software Validation of Medical Device to Meet FDA Requirements

    This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation. How software requirements are used in validation will be described. This course is not a programming course. We will discuss what must be done but will not discuss methods to execute necessary 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/SOFTWARE-VALIDATION-MEDICAL-DEVICE-501884/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 36 Request Info

    Webinar On 21 CFR Part 11 and Annex 11 Compliance - Specifics Needed to Eliminate 483s

    It is quite common between departments or individuals to neglect seeing the importance of 21 CFR Part 11 and Annex 11 (ERES) Compliance. Non-QA trained personnel or those that have no direct or have indirect contact with GxP systems fail to see the consequences of their actions or that of their department.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/21CFR-PART-11-ANNEX-11-COMPLIANCE-501871/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 37 Request Info

    Webinar On Reducing Risk in Third Party Relationships in the Financial Industry

    This webinar will prepare your organization to incorporate the best practices that should drive the use of third-parties. Participants will learn techniques of reducing risk in third-party relationships. An FI should adopt risk management processes commensurate with the level of risk and complexity of its third party relationships and should assure that comprehensive risk management and oversight of third party relationships involving critical activities reduce risk based on best practices.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/THIRD-PARTY-RELATIONSHIPS-FINANCIAL-INDUSTRY-501856/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 38 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
  • 39 Request Info

    Webinar On FDA's Two New Draft Guidance on Software and Device Changes and the 510(k)

    This course is intended to provide an overview of 2 new FDA draft guidance documents that clarify when medical device and software manufacturers must file a 510(k) (premarket notification) for changes to an existing device and/or software integrated with a device.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/FDAs-SOFTWARE-DEVICE-510k-501790/OCTOBER-2016-ES-TRAININGREGISTRY
  • 40 Request Info

    Webinar On Software Quality Assurance - How to Achieve Better Results

    With software quality becoming a central topic shaping the professional discussion in various industries, knowledge about QA best practices is becoming more and more valuable. In a fast-advancing technology landscape, companies that are able to consistently develop high quality, reliable and safe applications, and use mature processes while being able to react to changes have a competitive advantage over less responsive players. Attend this webinar to learn more about modern QA best practices.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/SOFTWARE-QUALITY-ASSURANCE-501779/OCTOBER-2016-ES-TRAININGREGISTRY