Seminar "Medical Device Regulatory Affairs"

Learning objectives

This two-day seminar is designed for English speaking professionals that have to navigate and comply with the complex medical devices regulations and approval processes. The goals of the seminar are:

  • Regulatory framework: The participants are aware of the relevant regulations, directives, guidelines, laws and standards and the interdependencies. The understand the major changes the EU regulations (MDR, IVDR) introduce in comparison to the EU directives.
  • Medical device approval: The participants know the different approval processes in the EU and the US, the respective preconditions such as quality management systems and the dependency of these processes on medical device classification.
  • Medical device software and IEC 62304: The participants understand the requirements laid out by IEC 62304, know how to compile a software requirements specification and a software architecture. They can explain core concepts such as software safety classification and SOUP and have an understanding how to
  • Risk Management and ISO 14971: The participants can precisely use the terms harm, hazard, hazardous situation, risk and severity. They know how the risk acceptance matrix and clinical evaluation have to interact. They have an understanding of the most relevant techniques for risk analysis (PHA, FMEA, FTA) and know options for risk control.
  • Cybersecurity: The participants understand how risk analysis and cybersecurity / vulnerability analysis work together and know how the cybersecurity related activities can be woven into the software development process.

The seminar is a best-of Johner Institute seminars that has been compiled for an English-speaking audience.

Target Group

The seminar explicitly addresses:

  • Project and product managers for active medical devices
  • System and software developers, system and software architects
  • Regulatory affairs manager
  • Quality manager

The seminar is also suitable for persons that are new to regulatory affairs and/or medical device software development.

Additional information

22.05.2019
-
23.05.2019         
Seminar “Best of in English”     

Luca Salvatore
Oskar Fürleger

Konstanz    

1360 € (excl. VAT)    1618,40 €

Agenda

Day 1: Focus Regulatory Framework, IEC 62304

TimeTopic
09:00Welcome, Expectations
09:20Introduction
09:45Regulatory Landscape, Directives (e.g. MDD), Regulations (e.g. MDR), Standards

10:30

Coffee Break

10:45Software as a Medical Device: Classifications, Examples, Artificial Intelligence
11:15Conformity Assessment in Europe and Market Approval in the US (focus: Software)
11:45Overview IEC 62304, Requirements Specification (1/2)

12:30

Lunch Break

13:30Overview IEC 62304, Requirements Specification (2/2)
14:00Software Architecture, SOUP versus OTS

15:00

Coffee Break

15:15Software Safety Classification and Interdependency with Risk Management
15:45Software Development Process, Agile Development
16:30Special Topics, Wrap-up, Q&A Session

17:00

End

Agenda of Day 2: Focus Risk Management, Cybersecurity, Special Topics

TimeTopic
09:00Welcome, Expectations (Update)
09:15Risk Management: Introduction, Basics, Definitions
10:00Risk Management: Risk Acceptance

10:30

Coffee Break

10:45Risk Analysis
11:15Risk Control
11:45Risk Management Process, ISO 14971, Documentation

12:15

Lunch Break

13:15Cybersecurity: Introduction, Basis, Regulations, Model
13:45Cybersecurity: Vulnerability Analysis, Threat Modeling
14:15Cybersecurity as Part of the Development Life Cycle, IT Security Guideline

14:45

Coffee Break

15:00Special Topics e.g. Usability & Requirements Engineering, Artificial Intelligence
16:30Wrap-up, Q&A Session

17:00

End