Updated training

content/home/training.md

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+---
+widget: "accomplishments"  
+headless: true  
+weight: 45
+
+title: "Courses"
+
+date_format: "2006-01-02"
+
+item:
+- organization: "KEY2COMPLIANCE AB"
+  title: "Device Control Training"
+  date_start: "2019-09-16"
+  date_end: "2019-09-17"
+  description: >
+    Course content: 
+     - Introduction 
+     - Medical devices - EU
+     - Combination products
+     - Quality system strategy
+     - Design Controls
+     - Planning
+     - User needs -> Design input
+     - Risk management
+     - Design Output
+     - Design Review
+     - Design Verification
+     - Design Validation
+     - Design Transfer
+     - Design Changes
+     - Design Documentation ”DHF”
+
+- organization: "KEY2COMPLIANCE AB"
+  title: "Software development - regulatory requirements"
+  date_start: "2019-09-21"
+  date_end: "2019-09-23"
+  description: >
+  Course content: 
+  - EU Medical Device Regulation 
+  - FDA regulations 
+  - Good practice: SW lifecycle processes 
+  - 60601 with focus on chapter 14, contribution of SW to essential performance 
+  - 62304 - Software development lifecycle 
+  - Development For class C software 
+  - Short intro to risk management - ISO 14971 
+  - Software safety class 
+  - Software risk in relation to 62304 
+  - Concept cybersecurity 
+  - Cybersecurity risk management process 
+  - Agile SW development 
+  - GDPR/HIPAA 
+  - Tool validation 
+
+- organization: "medicaldeviceHQ"
+  title: "Risk Management for Medical Devices and ISO 14971:2019"
+  date_start: "2024-02-23"
+  description: >
+    Learning goals: 
+      - To understand the overall process of risk management and how to create safe medical devices.
+      - To strengthen the ability of participants to independently perform risk analysis, risk evaluation and risk control.
+      - To establish and increase knowledge on risk management tools and their differences, such as FMEA and P-FMEA.
+
+
+---