About
Design, development and manufacturing of medical devices, from class I to class III. Consulting on Quality Assurance and Regulatory Affairs ISO 13485 : 2016 certified company by French Notified Body GMED. Registered with the FDA.
Technologies
Outlook
Microsoft Office 365
Google Maps
Google Font API
Google Maps (Non Paid Users)
Mobile Friendly
WordPress.org
Android
Node.js
Remote
Keywords
affaires reglementaires
conseil en qualite
conception de dispositifs medicaux classe i a iii
medical equipment manufacturing
medical device testing
patient-specific devices
ce certification
product validation
quality management
medical device quality system
orthopedic implants
quality assurance
implant design
r&d services
b2b
manufacturing
product development
ce marking
medical device certification
healthcare
medical device registration
surgical instruments
iso 13485
design for manufacturing
medical device innovation
implantable prostheses
project management
minimally invasive surgery
iso 14971
regulatory strategy
Company Information
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Employees 6
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Founded 2006
Location
44C Rue de Bray, Cesson-Sevigne, Brittany, France, 35510
