ISO Medical Device Industry

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  • 21 Request Info

    Webinar On Validation of a HPLC/UPLC Methodology

    Instrumental liquid chromatography (HPLC method development/ UPLC method development) commonly used in the pharmaceutical, environmental, and other areas for analyses needs to comply with either Good Laboratory Practices or ISO 17025 training. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 22 Request Info

    Webinar on New ISO Standard for Medical Device Quality Systems 13485: 2016 Summary of its Impact to the Medical Device Industry Professionals

    You will gain a thorough insight into the specific quality system requirements of all new International ISO 13485:2016 Quality System Standard requirements for Medical Devices. This timely and extremely informative webinar will truly build your knowledge from the fundamental quality principles. It will help you grow into fulfilling the quality and regulatory requirements as a professional working for medical device manufacturers of fully assembled devices and global suppliers manufacturing critical parts for the medical device industry. All noteworthy changes implemented into this key international standard will be discussed to pave the path for implementation of the changes in your organization. Price :- $250 Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 23 Request Info

    Developing Documents and Records to meet the Requirement of ISO

    QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the "what to do" component of a QMS. What is also needed are the "how to do it" or procedures and methods and finally the controls or evidence that it was done properly. GlobalCompliancePanel Refer a Friend Program: Any Customer to 3 Referrals "Can Participate 2 Days Seminar for free of Cost
  • 24 Request Info

    Webinar on ISO 14971-Incorporating Risk Management throughout the Product Life-cycle

    A key process for all medical device companies is product risk management. While this webinar focuses on the application of risk management to product outlined in ISO 14971:2007, we will also discuss the risk-based approach outlined in ISO 13485:2016. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 25 Request Info

    Webinar on Monitoring and Measuring Customer Satisfaction Using ISO 10004:2012

    The ISO 10004:2012 model has four major elements in the customer satisfaction process: Identifying customer expectations, gathering data, analyzing the data, and communicating the information. The webinar explores each element and explains its application. The webinar also discusses the difference between a complaint in the regulatory realm and a complaint involving only customer satisfaction.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 26 Request Info

    Webinar on ISO 13485:2016 - What's Changing and What It Means for Medical Device Companies

    This webinar focuses on what quality managers, quality system engineers, quality auditors and other personnel involved in quality system implementation will want to know about the upcoming revision and strategies of ISO 13485. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 27 Request Info

    Understanding ISO 13485 and its Relation to FDA's Quality Systems Regulation by Jessica Czamanski

    Areas Covered in the Webinar: Concept of quality management system All clauses in ISO 13485 Auditable clauses of ISO 13485 All parts of the FDA’s QSR Who is responsible for complying with QSR Differences between ISO 13485 and QSR Role of management in quality Exclusions from specific parts of the regulation or standard Internal audit requirement Who Will Benefit: Medical device manufacturers R&D teams for medical devices Personnel involved in the packaging of medical devices and packaging engineers Inventory control personnel in a medical device company Quality personnel and quality engineers Suppliers to medical device companies Biomedical engineers Manufacturing engineers
  • 28 Request Info

    ISO 9000:2000 Internal Auditing Course

    ISO 9000:2000 INTERNAL AUDITOR Training,1-3 days,What are changes to theISO 9000:2000?,What to Look For As an Auditor,Auditing Techniques,Developing a Checklist,Questioning Techniques&Perform an actual audit.