BEGIN:VCALENDAR VERSION:2.0 PRODID:-//PYVOBJECT//NONSGML Version 1//EN BEGIN:VTIMEZONE TZID:Europe/Stockholm BEGIN:STANDARD DTSTART:20001029T030000 RRULE:FREQ=YEARLY;BYDAY=-1SU;BYMONTH=10 TZNAME:CET TZOFFSETFROM:+0200 TZOFFSETTO:+0100 END:STANDARD BEGIN:DAYLIGHT DTSTART:20000326T020000 RRULE:FREQ=YEARLY;BYDAY=-1SU;BYMONTH=3 TZNAME:CEST TZOFFSETFROM:+0100 TZOFFSETTO:+0200 END:DAYLIGHT END:VTIMEZONE BEGIN:VEVENT UID:20260808T054201Z - 101@odoo-6c455687b8-9vjd8 DTSTART;TZID=Europe/Stockholm:20261125T090000 DTEND;TZID=Europe/Stockholm:20261126T160000 CREATED:20260808T054201Z DESCRIPTION:Me dical device software process design based on IEC 62304 \nThis course focuses on how to design a process for the development and maintenance of medical device software according to the IEC 62304 standard and the regula tory requirements that apply to medical device software. TopicsCurrent sof tware practicesDesigning high quality software in a regulated environmentS tandards for regulatory complianceImplementation examples for achieving co mpliancePractical applications of the requirements of the 62304 standardSo me possible future changes within the medical device software field Target group This course is targeted towards professionals working with the deve lopment of medical devices containing software or software as a medical de vice (SaMD)\, with risk assessment of software-based products\, quality as surance\, process improvements\, with the purchasing of software developme nt from subcontractors\, or purchasing software components. Educational go als After the course\, participants will have an understanding of how to e mploy design processes for medical device development based on the 62304 s tandard\, in order to achieve regulatory compliance and how to design high quality software in a regulated environment. Recommended prior knowledge A basic understanding of the medical device regulations and some product a nd software development experience is recommended. ​ Course presentation s Course material will be in English\, verbal presentation in English. Cou rse leaders The training is conducted in collaboration with Aurevia. Pleas e note: Intertek operates under strict standards of independence\, imparti ality\, and integrity. Read more about how we work here: https://www.inter tek.com/about/co​mpliance-governance/ Upcoming classes See all Your Dyna mic Snippet will be displayed here... This message is displayed because yo u did not provide both a filter and a template to use. DTSTAMP:20260808T054201Z LOCATION:Intertek Semko AB\, Torshamnsgatan 43\, Kista 16440\, Sweden SUMMARY:Medical device software process design based on IEC 62304 X-ALT-DESC;FMTTYPE=text/html:Medical device software process design based on IEC 62304 < /a>\nThis course focuses on how to design a process for the development an d maintenance of medical device software according to the IEC 62304 standa rd and the regulatory requirements that apply to medical device software. TopicsCurrent software practicesDesigning high quality software in a regul ated environmentStandards for regulatory complianceImplementation examples for achieving compliancePractical applications of the requirements of the 62304 standardSome possible future changes within the medical device soft ware field Target group This course is targeted towards professionals work ing with the development of medical devices containing software or softwar e as a medical device (SaMD)\, with risk assessment of software-based prod ucts\, quality assurance\, process improvements\, with the purchasing of s oftware development from subcontractors\, or purchasing software component s. Educational goals After the course\, participants will have an understa nding of how to employ design processes for medical device development bas ed on the 62304 standard\, in order to achieve regulatory compliance and h ow to design high quality software in a regulated environment. Recommended prior knowledge A basic understanding of the medical device regulations a nd some product and software development experience is recommended. ​ Co urse presentations Course material will be in English\, verbal presentatio n in English. Course leaders The training is conducted in collaboration wi th Aurevia. Please note: Intertek operates under strict standards of indep endence\, impartiality\, and integrity. Read more about how we work here: https://www.intertek.com/about/co​mpliance-governance/ Upcoming classes See all Your Dynamic Snippet will be displayed here... This message is dis played because you did not provide both a filter and a template to use. END:VEVENT END:VCALENDAR