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:20260831T085953Z - 81922@odoo-57766ccd69-mgjlj
DTSTART;TZID=Europe/Stockholm:20260915T090000
DTEND;TZID=Europe/Stockholm:20260915T163000
CREATED:20260831T085953Z
DESCRIPTION:<a href="https://ido.intertek.com/event/iec-en-61010-1-electric
 al-equipment-for-measurement-control-and-laboratory-use-102/register">IEC/
 EN 61010-1\; Electrical equipment for measurement\, control and laboratory
  use</a>\nAll companies selling products on the European market must be ab
 le to demonstrate that their products meet the applicable EU requirements.
  The IEC/EN 61010-1 standard has been developed to specify the requirement
 s for measurement\, control and laboratory equipment. In this training we 
 will go through the requirements. Almost a 100 percent of all measurement\
 , control and laboratory equipment that is submitted for testing today doe
 s not meet the requirements on the first try! To discover this at the end 
 of the development process can be very costly. For the manufacturer\, this
  means that the product must be redesigned. The consequences are delayed m
 arket entry\, lost sales and the cost of redesigning and retesting the pro
 duct. Our training in IEC/EN 61010-1 edition 3.1 helps you understand the 
 requirements that are placed on your product during testing to fulfill the
  requirements. All manufacturers selling products on the European market h
 ave to be able to demonstrate that the products meet the applicable EU req
 uirements. As a manufacturer of measurement\, control and laboratory equip
 ment\, you must be able to demonstrate that the product meets EU requireme
 nts\, including the Low Voltage Directive (LVD)\, in some cases the Medica
 l Devices Regulation (MDR) and in other In Vitro Diagnostic Regulation (IV
 DR) and in many cases also the Machinery Directive (MD). By meeting the re
 quirements of the harmonized standard IEC/EN 61010-1\, which was developed
  to specify the requirements for measurement\, control and laboratory equi
 pment\, the product is assumed to meet the current directives. If you also
  want to sell the product in North America\, there are several additional 
 requirements that the product must meet. About the course The IEC 61010-1 
 training course initially and briefly covers issues of product liability a
 nd CE marking as well as the several directives that IEC 61010 [...]
DTSTAMP:20260831T085953Z
SUMMARY:IEC/EN 61010-1\; Electrical equipment for measurement\, control and
  laboratory use
X-ALT-DESC;FMTTYPE=text/html:<a href="https://ido.intertek.com/event/iec-en
 -61010-1-electrical-equipment-for-measurement-control-and-laboratory-use-1
 02/register">IEC/EN 61010-1\; Electrical equipment for measurement\, contr
 ol and laboratory use</a>\nAll companies selling products on the European 
 market must be able to demonstrate that their products meet the applicable
  EU requirements. The IEC/EN 61010-1 standard has been developed to specif
 y the requirements for measurement\, control and laboratory equipment. In 
 this training we will go through the requirements. Almost a 100 percent of
  all measurement\, control and laboratory equipment that is submitted for 
 testing today does not meet the requirements on the first try! To discover
  this at the end of the development process can be very costly. For the ma
 nufacturer\, this means that the product must be redesigned. The consequen
 ces are delayed market entry\, lost sales and the cost of redesigning and 
 retesting the product. Our training in IEC/EN 61010-1 edition 3.1 helps yo
 u understand the requirements that are placed on your product during testi
 ng to fulfill the requirements. All manufacturers selling products on the 
 European market have to be able to demonstrate that the products meet the 
 applicable EU requirements. As a manufacturer of measurement\, control and
  laboratory equipment\, you must be able to demonstrate that the product m
 eets EU requirements\, including the Low Voltage Directive (LVD)\, in some
  cases the Medical Devices Regulation (MDR) and in other In Vitro Diagnost
 ic Regulation (IVDR) and in many cases also the Machinery Directive (MD). 
 By meeting the requirements of the harmonized standard IEC/EN 61010-1\, wh
 ich was developed to specify the requirements for measurement\, control an
 d laboratory equipment\, the product is assumed to meet the current direct
 ives. If you also want to sell the product in North America\, there are se
 veral additional requirements that the product must meet. About the course
  The IEC 61010-1 training course initially and briefly covers issues of pr
 oduct liability and CE marking as well as the several directives that IEC 
 61010 [...]
END:VEVENT
END:VCALENDAR