jcktrue.dk/content/home/training.md

widget, headless, weight, title, date_format, item

widget	headless	weight	title	date_format	item
accomplishments	true	45	Courses	2006-01-02	organization title date_start date_end description KEY2COMPLIANCE AB Device Control Training 2019-09-16 2019-09-17 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 title date_start date_end description Course content KEY2COMPLIANCE AB Software development - regulatory requirements 2019-09-21 2019-09-23 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 title date_start description medicaldeviceHQ Risk Management for Medical Devices and ISO 14971:2019 2024-02-23 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.