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DMD Consulting - Medical devices

DMD Consulting - Medical devices

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DMD Consulting - Medical devices | mddconsulting.eu Reviews
<META>
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DMD Consulting - Medical devices
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KEYWORDS
1 Medical device
2 Regulatory
3 Medical device directive
4 Quality management systems
5 US/FDA Code of Federal Regula tion
6 Euro pean Union Medical Devices Directives
7 CE marking
8 Technical File
9 Post-market surveillance
10 Software validation
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poul schmidt andersen,e mail psa@mddconsulting eu,liselotte blond sørensen,e mail lbs@mddconsulting eu,e mail info@mddconsulting eu
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DMD Consulting - Medical devices | mddconsulting.eu Reviews

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DMD Consulting - Medical devices

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Regulatory compliance services regarding requirements of the US, Canadian. And EU markets . Europe can benefit from local assistance with respect to US product submission requirements, particularly for implants, sterile devices or devices containing software. Companies who wishes to marketing their medical devices in. EU Authorized Representative Services. DMD Consulting provides compliance services regarding process -and software validation requirements of the US, Canadian and EU markets. Harmonized sta...

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DMD Consulting - Medical devices

http://www.mddconsulting.eu/default.asp

Software Validation / Introdution to EN 62304. 28 February to 29 February 2012. Medical Device Sterilization for Manufacturers. 23 April to 27 April 2012. Medical Devices Consulting aps. The Danish Cancer Society. Phone: 45 4499 0023.

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