Dear Colleagues,
I have some free capacity to support manufacturers in the preparation for compliance with the new European Medical Device Regulation, especially in the following areas:
• 1 day workshop about the ongoing changes
• design process
• postmarket surveillance, device vigilance
• postmarket clinical follow-up
• risk management
• clinical evaluation
• packaging material development
• quality management, including internal audit.
Should you see opportunities, please let me know.
Regards
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Peter Mikó M.D
ArtPharm Ltd.
Gyermely
Hungary
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