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Session two of the Electro-Medical Device webinar series will sort through EN50581 and the different specifications that need to be followed in order demonstrate compliance to the hazardous materials restricted by EU Directive 2011/65/EU

Starts

Jul 16, 2014

Ends

Jul 16, 2014

Location

Online

Body Scan X-ray

Session two of the Electro-Medical Device webinar series will sort through EN50581 and the different specifications that need to be followed in order demonstrate compliance to the hazardous materials restricted by EU Directive 2011/65/EU.

This webcast will review some of the essential elements of the standard paying close attention to and answering some of the questions specific to clause 4.3.2 Supplier and Material Assessment, clause 4.3.3  Documents for Materials, Parts,  and/or Sub-Assemblies and clause 4.3.4 Evaluation of Quality and Trustworthiness of Suppliers and Data.

Topics will include:

  • Content of the Technical Documentation File
  • Supplier & material confidence assessment
  • Evaluation of quality and trustworthiness

Event Details:

Time: 3:00 – 3:30 pm Eastern Time

Cost: No Charge

 

CLICK HERE to view all of the other topics in this Electronic Medical Devices Webinar Series!