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I3CGlobal (IN)
Medical device regulatory consulting firm
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About Us
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ISO 13485 (MDQMS)
FDA Audit
GMP Certificate
FDA QSR 21 CFR Part 820
Medical Device Single Audit Program (MDSAP)
Medical Device Facility Design
EUROPE
CE MARKING – The EU Medical Device Regulation [MDR]
IVDR CE MARKING
Medical Device Clinical Evaluation
EC Representative (EC Rep)
INDIA
Medical Device Regulation
Manufacturing License
Medical Device Import License
Medical Device Test License
Post Approval Changes
UK
UKCA Certification
UK Responsible Person
USA
US FDA 510(k)
FDA Registration & Listing
News
Contact
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Home
About Us
Services
ISO 13485 (MDQMS)
FDA Audit
GMP Certificate
FDA QSR 21 CFR Part 820
Medical Device Single Audit Program (MDSAP)
Medical Device Facility Design
EUROPE
CE MARKING – The EU Medical Device Regulation [MDR]
IVDR CE MARKING
Medical Device Clinical Evaluation
EC Representative (EC Rep)
INDIA
Medical Device Regulation
Manufacturing License
Medical Device Import License
Medical Device Test License
Post Approval Changes
UK
UKCA Certification
UK Responsible Person
USA
US FDA 510(k)
FDA Registration & Listing
News
Contact
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