BEGIN:VCALENDAR VERSION:2.0 PRODID:-//Exida: Excellence. Independence. International Customer Base.//NO NSGML kigkonsult.se iCalcreator 2.30.10// CALSCALE:GREGORIAN METHOD:PUBLISH UID:1c6b7adb-1401-4a53-8a76-9fd7a7947e12 X-WR-CALNAME:iCagenda X-WR-CALDESC:Event Management Extension for Joomla! X-WR-RELCALID:3E26604A-50F4-4449-8B3E-E4F4932D05B5 X-WR-TIMEZONE:Europe/Rome BEGIN:VTIMEZONE TZID:Europe/Rome BEGIN:STANDARD TZNAME:CET DTSTART:20241027T030000 TZOFFSETFROM:+0200 TZOFFSETTO:+0100 RDATE:20251026T030000 RDATE:20261025T030000 END:STANDARD BEGIN:DAYLIGHT TZNAME:CEST DTSTART:20250330T020000 TZOFFSETFROM:+0100 TZOFFSETTO:+0200 RDATE:20260329T020000 RDATE:20270328T020000 END:DAYLIGHT END:VTIMEZONE BEGIN:VEVENT UID:dac644a3-eb74-4dcb-a1b8-bc81240e83dd DTSTAMP:20260404T134644Z CATEGORIES:Cybersecurity CLASS:PUBLIC DESCRIPTION;ALTREP="CID:": \n\n\n\n\n\nJoin our Training and learn the Cybersecurity Essentials for M edical Device Development\n\n\n\n \nAgenda and Content\n\n\n\n\n\nWelcome\ , Introduction\, Training Goals\nCybersecurity Threat Landscape: Why It Ma tters for Medical Devices\nRegulatory Frameworks &\; Standards\, e.g.: \n\nMedical Device Regulation (MDR)\nCyber Resilience Act (CRA)\nNetwork a nd Information Security Directive 2 (NIS2)\nFDA Guidance\nISO 14971\nIEC 8 1001-5-1\nIEC TR 60601-4-5\nIEC 62443\n\n\nSecure Development Lifecycle - Risk Management &\; Security Governance\nThreat Modelling and Security Levels\nSecurity Requirements\nSecure Software Development Fundamentals\n \nSW Exploitation\nTechnical Controls and Secure Architecture\nCoding Guid elines\nSW Toolchain\n\n\nValidating Device Security: Tools and Techniques for Testing\nHardware &\; Embedded Security\nPost-Market Security - Vu lnerability Handling &\; Incident Response\nPitfalls &\; Lessons Lea rned from Real Incidents\nQ&\;A and Wrap-Up\n\nAs medical devices becom e more connected\, cybersecurity is critical for ensuring patient safety a nd regulatory compliance.\nThis expert-led training provides an overview o f medical device cybersecurity and equips R&\;D\, QA\, and regulatory t eams with the tools to integrate cybersecurity into the full medical devic e development lifecycle.\nWho should attend?\nEngineers\, who want to lear n more about cybersecurity related to medical device development\, such as :\n\nMedical Device Software Developers &\; Engineers\nSystems Architec ts\nCybersecurity Specialists / Product Security Engineers\nQuality Assura nce (QA) &\; Test Engineers\nRegulatory Affairs Professionals\nRisk Man agement &\; Safety Engineers\n\nBasic experience in cybersecurity and f unctional safety is beneficial but not required.\nFor more details about t he course topics\, download the brochure on the top of the page\n\n\nDurat ion: 2 half-days\n \nSchedule: 1st day from 2PM to 6PM\; 2nd day from 2PM to 6PM\;\n \nPrice: 790€\;\nLanguage: English or German in agreement with the participants. The training material will be in English.\nLocation: ONL INE. Customer specific on-site or online trainings are also possible – jus t get in touch!\nCertificate: each participant gets a letter of attendance .\n\n\n DTSTART:20251020T120000Z DTEND:20251021T160000Z GEO:00;0 LOCATION:Prof.-Messerschmitt-Straße 1 D-85579 Neubiberg / Germany ORGANIZER;CN=:kerstin.tietel@exida.com SEQUENCE:1 SUMMARY:Cybersecurity for Medical Device Development (DE0641) TRANSP:OPAQUE URL:https://www.exida-eu.com/all-trainings/cybersecurity/285-cybersecurity- for-medical-device-development-de0641 END:VEVENT END:VCALENDAR