Risk Management of Medical Device Software According to ISO 14971

• Medical device manufacturers whose products contain software or are a standalone software product.
• Employees who are in charge of:
  • Regulatory affairs management
  • Quality management and risk management
  • IT management
  • Usability, requirements, system and software engineering
  • Project and product management
  • Corporate management
  • Service providers and suppliers in medical device industry
  • Consultants of medical software

• Risk management basics, definitions of terms
• Risk management process and ISO 14971
• Risk management analysis and documentation requirements
• Risk analysis for software:
  • Scenario based risk analysis, SW-architecture, root-cause analysis,
  • FTA, FMEA, IT security-analysis and third-party components
  • Concept of EC/TR 80002-1:2009 - Medical device software Part 1:
  • Guidance on the application of ISO 14971 to medical device software
• Risk assessment and risk management report
• Production and post-production activities, (configuration management, deployment, updates of databases, operating systems etc.)
• Change Management and risks
• Normative requirements according to ISO/EN ISO 14971, to FDA, to MDR and ISO/TR 24971: Medical devices - Guidance on the application of ISO 14971

Medical device software is software that is intended to be used, alone or in combination, for a purpose as specified in the definition of a “medical device” in the MDR or IVDR, regardless of whether the software is independent (standalone software) or driving or influencing the use of a device (embedded software as part of a medical device). The software has to be designed to ensure reliability and performance according to their intended use.

The establishment of an interactive risk management process across the product lifecycle is very essential for every manufacturer of medical device software in order to eliminate risks or minimize them as much as possible. Thereby, it is important to take applicable standards into account and consider various risk aspects, such as effects of software errors, negative interactions, aspects of the IT environment and IT security, safety-relevant functions and processes or verification- and validation steps.

In this seminar, you will learn the basic requirements for risk analysis of medical device software according to the applicable standards and you will be able to carry out a risk analysis and document the results properly. You will be able to assess the risks in your software and create a risk management report based on this.

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This seminar addresses internationally valid standards. The contents of the seminar correspond to the current status of the revision/harmonization.

• Instructor-led in a virtual classroom
• Course delivered by one of TÜV SÜD's leading industry experts
• Small class sizes enhance trainer-delegate relationship
• Receive globally recognised TÜV SÜD certificate upon completion

Instructor-led training in a virtual classroom. This means the course is Live Online. Participants will learn through online teaching. Lectures, case studies, group exercises, discussions, problem solving, examples with explanation, assignments and/or quizzes happen in the virtual classroom training. Participants need to connect to the class from any internet accessible location. Each module is delivered live using webinar technology, creating a virtual classroom learning environment. Live sessions provide you with direct access to the trainer so you can ask questions, understand complex concepts and share ideas with peers. Webcam and microphone are REQUIRED to interact with the instructor and/or other participants.

The course content and structure are designed by the domain experts from TÜV SÜD. With immense experience and knowledge in the relevant standards, our team of product specialists and technical experts at TÜV SÜD, developed the course content based on current business landscape and market requirements.