Learn about Risk Management and the processes for identifying, evaluating, and mitigating hazards associated with the use of medical devices. 

    Duration: 16 hours

    Modality: Group

    Participant limit: 15

    Technical Information

      The purpose of this course is to provide students with the knowledge and hands-on experience in the elements of process and product control that a Quality Engineer should excel. 

      Duration: 24 hours

      Modality: Group

      Participant limit: 15

      Technical Information

        This course is designed to provide participants with a solid understanding of the fundamentals of action planning and management as part of a CAPA.

        Duration: 9 hours

        Modality: Group 

        Participant limit: 15

        Technical Information

          This course is designed to provide medical device industry professionals with the skills necessary to effectively and accurately complete CAPA investigation reports.

          Duration: 12 hours

          Modality: Group 

          Participant limit: 15

          Technical Information

            Learn the tools and practical experience to correctly define problems, identify root causes and implement solutions.

            Duration: 12 hours

            Modality: Group

            Participant limit: 15

            Technical Information

              The purpose of this curse is to provide students with the knowledge and hands-on experience in the elements of process and product control that a Quality Engineer should excel.

              Duration: 6 hours

              Modality: Group 

              Participant limit: 15

              Technical Information