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BEGIN:VEVENT
UID:20260808T045541Z - 20723@odoo-6c455687b8-9vjd8
DTSTART;TZID=Europe/Stockholm:20260915T090000
DTEND;TZID=Europe/Stockholm:20260915T163000
CREATED:20260808T045541Z
DESCRIPTION:<a href="https://18-0-staging.intertek.test.cloudworkz.eu/event
 /iec-en-61010-1-electrical-equipment-for-measurement-control-and-laborator
 y-use-46/register">IEC/EN 61010-1\; Electrical equipment for measurement\,
  control and laboratory use</a>\nAll companies selling products on the Eur
 opean market must be able to demonstrate that their products meet the appl
 icable EU requirements. The IEC/EN 61010-1 standard has been developed to 
 specify the requirements for measurement\, control and laboratory equipmen
 t. In this training we will go through the requirements. Almost a 100 perc
 ent of all measurement\, control and laboratory equipment that is submitte
 d for testing today does not meet the requirements on the first try! To di
 scover this at the end of the development process can be very costly. For 
 the manufacturer\, this means that the product must be redesigned. The con
 sequences are delayed market entry\, lost sales and the cost of redesignin
 g and retesting the product. Our training in IEC/EN 61010-1 edition 3.1 he
 lps you understand the requirements that are placed on your product during
  testing to fulfill the requirements. All manufacturers selling products o
 n the European market have to be able to demonstrate that the products mee
 t the applicable EU requirements. As a manufacturer of measurement\, contr
 ol and laboratory equipment\, you must be able to demonstrate that the pro
 duct meets EU requirements\, including the Low Voltage Directive (LVD)\, i
 n some cases the Medical Devices Regulation (MDR) and in other In Vitro Di
 agnostic Regulation (IVDR) and in many cases also the Machinery Directive 
 (MD). By meeting the requirements of the harmonized standard IEC/EN 61010-
 1\, which was developed to specify the requirements for measurement\, cont
 rol and laboratory equipment\, 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 and CE marking as well as the several directives tha
 t IEC 61010 [...]
DTSTAMP:20260808T045541Z
SUMMARY:IEC/EN 61010-1\; Electrical equipment for measurement\, control and
  laboratory use
X-ALT-DESC;FMTTYPE=text/html:<a href="https://18-0-staging.intertek.test.cl
 oudworkz.eu/event/iec-en-61010-1-electrical-equipment-for-measurement-cont
 rol-and-laboratory-use-46/register">IEC/EN 61010-1\; Electrical equipment 
 for measurement\, control and laboratory use</a>\nAll companies selling pr
 oducts on the European market must be able to demonstrate that their produ
 cts meet the applicable EU requirements. The IEC/EN 61010-1 standard has b
 een developed to specify the requirements for measurement\, control and la
 boratory 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 manufacturer\, this means that the product must be re
 designed. The consequences are delayed market entry\, lost sales and the c
 ost of redesigning and retesting the product. Our training in IEC/EN 61010
 -1 edition 3.1 helps you understand the requirements that are placed on yo
 ur product during testing to fulfill the requirements. All manufacturers s
 elling products on the European market have to be able to demonstrate that
  the products meet the applicable EU requirements. As a manufacturer of me
 asurement\, control and laboratory equipment\, you must be able to demonst
 rate that the product meets EU requirements\, including the Low Voltage Di
 rective (LVD)\, in some cases the Medical Devices Regulation (MDR) and in 
 other In Vitro Diagnostic Regulation (IVDR) and in many cases also the Mac
 hinery Directive (MD). By meeting the requirements of the harmonized stand
 ard IEC/EN 61010-1\, which was developed to specify the requirements for m
 easurement\, control and laboratory equipment\, 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 brie
 fly covers issues of product liability and CE marking as well as the sever
 al directives that IEC 61010 [...]
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