Medical Device Regulatory Consulting - I3CGLOBAL

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• I 3 Consulting | CE Marking | FDA Registration | Medical Device

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• About Us - about us | i 3 consulting

  A GMP expert. Provided GMP consultancy for various Medical Device, Stem cell Research, and Pharmaceuticals companies across China, Morocco, Srilanka and India.

• World-Class Regulatory Consulting Services- I3CGLOBAL

  I3CGLOBAL is a vibrant and customer-focused company that provides medical device regulatory consulting services for US, EU & India.

• USFDA | Class 1 | Class 11 | Class 111 | Medical Device Classification

  How to find Class of Medical Device as per US FDA:

• FDA Drug Establishment Registration |US FDA Cosmetic Establishment Registration

  We are US FDA regulatory consultants providing the following services. Our US FDA services are fast and economical. Offices In India and USA :

• Classification of Medical Device - Medical Device Classification

  The classification of medical devices in the European Union is outlined in Annex IX of the Council Directive 93/42/EEC: