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:20260831T094504Z - 23206@odoo-57766ccd69-mgjlj DTSTART;TZID=Europe/Stockholm:20261020T090000 DTEND;TZID=Europe/Stockholm:20261020T160000 CREATED:20260831T094504Z DESCRIPTION:Basic course in IEC 60601-1\, Ed. 3.2\nLearn how to use IEC 60601-1\, Ed. 3.2 in an effective way. Nearly all medical devices tested to IEC 60601-1 Ed 3.2 fail to comply with the standard requ irements of the first submission. Just as many are rejected on their Risk Management File. In-depth knowledge of the standard is a must to mitigate this risk. Failing compliance testing means redesigning the product and re working the Risk Management File (RMF). The consequence is delayed market entry\, lost sales\, and high redesign costs\, all of which can be avoided by learning about the standard requirements. This course covers Technical requirements and safety philosophiesThe standardization process and the d evelopment history of the standardSafety requirements such asApplied parts Electrical hazards Mechanic hazardsFire hazardsTemperature hazardsComponen t requirementsInterpretations of requirements in the standardTest methods Course objectives After the course\, you should have a good knowledge of t he requirements that you as a manufacturer and your products must meet. Th is knowledge will help you minimize the risks of expensive development pro jects and to get your product to market faster. Target audience The course is primarily aimed at those who work with the development of medical devi ces. The course may also be of interest to those who work as quality manag ers or with regulatory affairs. Prior knowledge To get the most out of the training\, it is an advantage (but not essential) if you have read the st andard and have some experience of design and safety requirements. ​ Cou rse language English Please note: Intertek operates under strict standards of independence\, impartiality\, and integrity. Read more about how we wo rk here: https://www.intertek.com/about/co​mpliance-governance/ Course L eader Jenny Larsson Falk Technical Leader Medical and Laboratory Equipment Jenny Larsson Falk is Technical Leader within [...] DTSTAMP:20260831T094504Z SUMMARY:Basic course in IEC 60601-1\, Ed. 3.2 X-ALT-DESC;FMTTYPE=text/html:Basic course in IEC 60601-1\, E d. 3.2\nLearn how to use IEC 60601-1\, Ed. 3.2 in an effective way. Ne arly all medical devices tested to IEC 60601-1 Ed 3.2 fail to comply with the standard requirements of the first submission. Just as many are reject ed on their Risk Management File. In-depth knowledge of the standard is a must to mitigate this risk. Failing compliance testing means redesigning t he product and reworking the Risk Management File (RMF). The consequence i s delayed market entry\, lost sales\, and high redesign costs\, all of whi ch can be avoided by learning about the standard requirements. This course covers Technical requirements and safety philosophiesThe standardization process and the development history of the standardSafety requirements suc h asApplied partsElectrical hazards Mechanic hazardsFire hazardsTemperatur e hazardsComponent requirementsInterpretations of requirements in the stan dardTest methods Course objectives After the course\, you should have a go od knowledge of the requirements that you as a manufacturer and your produ cts must meet. This knowledge will help you minimize the risks of expensiv e development projects and to get your product to market faster. Target au dience The course is primarily aimed at those who work with the developmen t of medical devices. The course may also be of interest to those who work as quality managers or with regulatory affairs. Prior knowledge To get th e most out of the training\, it is an advantage (but not essential) if you have read the standard and have some experience of design and safety requ irements. ​ Course language English Please note: Intertek operates under strict standards of independence\, impartiality\, and integrity. Read mor e about how we work here: https://www.intertek.com/about/co​mpliance-gov ernance/ Course Leader Jenny Larsson Falk Technical Leader Medical and Lab oratory Equipment Jenny Larsson Falk is Technical Leader within [...] END:VEVENT END:VCALENDAR