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:20261029T050632Z - 83784@odoo-54dc9f858c-c7xvh
DTSTART;TZID=Europe/Stockholm:20261202T090000
DTEND;TZID=Europe/Stockholm:20261202T163000
CREATED:20261029T050632Z
DESCRIPTION:<a href="https://package-1.intertek.test.cloudworkz.eu/event/ie
 c-en-61010-1-electrical-equipment-for-measurement-control-and-laboratory-u
 se-102/register">IEC/EN 61010-1\; Electrical equipment for measurement\, c
 ontrol and laboratory use</a>\nAll companies selling products on the Europ
 ean market must be able to demonstrate that their products meet the applic
 able EU requirements. The IEC/EN 61010-1 standard has been developed to sp
 ecify the requirements for measurement\, control and laboratory equipment.
  In this training we will go through the requirements. Almost a 100 percen
 t of all measurement\, control and laboratory equipment that is submitted 
 for testing today does not meet the requirements on the first try! To disc
 over this at the end of the development process can be very costly. For th
 e manufacturer\, this means that the product must be redesigned. The conse
 quences 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 help
 s you understand the requirements that are placed on your product during t
 esting 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 produ
 ct meets EU requirements\, including the Low Voltage Directive (LVD)\, in 
 some cases the Medical Devices Regulation (MDR) and in other In Vitro Diag
 nostic Regulation (IVDR) and in many cases also the Machinery Directive (M
 D). By meeting the requirements of the harmonized standard IEC/EN 61010-1\
 , which was developed to specify the requirements for measurement\, contro
 l and laboratory equipment\, the product is assumed to meet the current di
 rectives. If you also want to sell the product in North America\, there ar
 e several additional requirements that the product must meet. About the co
 urse The IEC 61010-1 training course initially and briefly covers issues o
 f product liability and CE marking as well as the several directives that 
 IEC 61010 [...]
DTSTAMP:20261029T050632Z
SUMMARY:IEC/EN 61010-1\; Electrical equipment for measurement\, control and
  laboratory use
X-ALT-DESC;FMTTYPE=text/html:<a href="https://package-1.intertek.test.cloud
 workz.eu/event/iec-en-61010-1-electrical-equipment-for-measurement-control
 -and-laboratory-use-102/register">IEC/EN 61010-1\; Electrical equipment fo
 r measurement\, control and laboratory use</a>\nAll companies selling prod
 ucts on the European market must be able to demonstrate that their product
 s meet the applicable EU requirements. The IEC/EN 61010-1 standard has bee
 n developed to specify the requirements for measurement\, control and labo
 ratory equipment. In this training we will go through the requirements. Al
 most a 100 percent of all measurement\, control and laboratory equipment t
 hat is submitted for testing today does not meet the requirements on the f
 irst try! To discover this at the end of the development process can be ve
 ry costly. For the manufacturer\, this means that the product must be rede
 signed. The consequences are delayed market entry\, lost sales and the cos
 t 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 your
  product during testing to fulfill the requirements. All manufacturers sel
 ling products on the European market have to be able to demonstrate that t
 he products meet the applicable EU requirements. As a manufacturer of meas
 urement\, control and laboratory equipment\, you must be able to demonstra
 te that the product meets EU requirements\, including the Low Voltage Dire
 ctive (LVD)\, in some cases the Medical Devices Regulation (MDR) and in ot
 her In Vitro Diagnostic Regulation (IVDR) and in many cases also the Machi
 nery Directive (MD). By meeting the requirements of the harmonized standar
 d IEC/EN 61010-1\, which was developed to specify the requirements for mea
 surement\, control and laboratory equipment\, the product is assumed to me
 et the current directives. If you also want to sell the product in North A
 merica\, there are several additional requirements that the product must m
 eet. About the course The IEC 61010-1 training course initially and briefl
 y covers issues of product liability and CE marking as well as the several
  directives that IEC 61010 [...]
END:VEVENT
END:VCALENDAR