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:20260808T054202Z - 87298@odoo-6c455687b8-9vjd8 DTSTART;TZID=Europe/Stockholm:20261020T090000 DTEND;TZID=Europe/Stockholm:20261020T160000 CREATED:20260808T054202Z DESCRIPTION:Basic course in IEC 60601 -1\, Ed. 3.2\nLearn how to use IEC 60601-1\, Ed. 3.2 in an effective w ay. Nearly 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 rejected on their Risk Management File. In-depth knowledge of the standard is a must to mitigate this risk. Failing compliance testing means redesig ning the product and reworking the Risk Management File (RMF). The consequ ence 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 standardiz ation process and the development history of the standardSafety requiremen ts such asApplied partsElectrical hazards Mechanic hazardsFire hazardsTemp erature hazardsComponent requirementsInterpretations of requirements in th e standardTest methodsCourse objectives After the course\, you should have a good knowledge of the requirements that you as a manufacturer and your products must meet. This knowledge will help you minimize the risks of exp ensive development projects and to get your product to market faster.Targe t audience The course is primarily aimed at those who work with the develo pment 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 the 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 r equirements.Course language English Please note: Intertek operates under s trict standards of independence\, impartiality\, and integrity. Read more about how we work here: https://www.intertek.com/about/co​mpliance-gover nance/ Course Leader Jenny Larsson Falk Technical Leader 61010 Jenny Larss on Falk is Technical Leader within Medical\, Laboratory and Measurement [. ..] DTSTAMP:20260808T054202Z SUMMARY:Basic course in IEC 60601-1\, Ed. 3.2 X-ALT-DESC;FMTTYPE=text/html:Basic co urse 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 requirements of the first submission. Just as many are rejected on their Risk Management File. In-depth knowledg e of the standard is a must to mitigate this risk. Failing compliance test ing means redesigning the product and reworking the Risk Management File ( RMF). The consequence is delayed market entry\, lost sales\, and high rede sign costs\, all of which can be avoided by learning about the standard re quirements. This course covers Technical requirements and safety philosoph iesThe standardization process and the development history of the standard Safety requirements such asApplied partsElectrical hazards Mechanic hazard sFire hazardsTemperature hazardsComponent requirementsInterpretations of r equirements in the standardTest methodsCourse objectives After the course\ , you should have a good knowledge of the requirements that you as a manuf acturer and your products must meet. This knowledge will help you minimize the risks of expensive development projects and to get your product to ma rket faster.Target audience The course is primarily aimed at those who wor k with the development of medical devices. The course may also be of inter est to those who work as quality managers or with regulatory affairs.Prior knowledge To get the most out of the training\, it is an advantage (but n ot essential) if you have read the standard and have some experience of de sign and safety requirements.Course language English Please note: Intertek operates under strict standards of independence\, impartiality\, and inte grity. Read more about how we work here: https://www.intertek.com/about/co ​mpliance-governance/ Course Leader Jenny Larsson Falk Technical Leader 61010 Jenny Larsson Falk is Technical Leader within Medical\, Laboratory a nd Measurement [...] END:VEVENT END:VCALENDAR