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Courses

  • 1 Request Info

    Webinar on Problem Solving - Root Cause Analysis in Pharma Manufacturing

    Join this webinar to understand relevant inspection steps in relation to Root Cause, how to use RCA to better effect, what RCA tools really, more. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Problem-Solving-Root-Cause-Analysis-in-Pharma-Manufacturing-503456/JULY-2018-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on Data Governance for Computer Systems Regulated by FDA

    The attendees will learn how to leverage best practices across all systems by creating a standardized program for FDA data governance. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Data-Governance-for-Computer-Systems-Regulated-by-FDA-502212/MAY-2018-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on Lyophilization: What you need to Know, Validation and Regulatory Approaches

    This webinar discusses how the lyophilization cycle and process is developed and validated, along with the FDA regulatory requirements for lyophilization. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Lyophilization-What-you-need-to-Know-Validation-and-Regulatory-Approaches-503313/MAY-2018-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Human Factors Usability Studies Following ISO 62366 and FDA Guidance

    This training program will examine how human factors/usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process and validating the effectiveness of the studies will be explained. The various types and methods of human factors analysis will be explained. This process conforms to the new ISO 62366 standard and the new FDA guidance document.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Human-Factors-Usability-Studies-Following-ISO-62366-and-FDA-Guidance-504868/JANUARY-2018-ES-TRAININGREGISTRY
  • 5 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
  • 6 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
  • 7 Request Info

    Webinar On Human Factors/Usability Based on ISO 62366

    This training program will examine how human factors/usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process, and validating the effectiveness of the studies will be explained. The various types and methods of human factors analysis will be explained. This process conforms to the new ISO 62366 standard and the new FDA guidance document.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-USABILITY-BASED-ISO-62366-501460/JULY-2016-ES-TRAININGREGISTRY