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I3CGLOBAL's Profile
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Our GMP Consulting Team will understand your product and design the facility according to international regulations. GMP consulting includes documenta...
Under the new MDR and IVDR, the EU representative fulfills important duties. The EC Rep acts as a legal interface between the manufacturer and the aut...
I3CGLOBAL is an award-winning regulatory consulting team specializing in the medical device domain. I3CGlobal assists Medical Device and Invitro Diagn...
I3CGLOBAL can help consult and assist in preparing to comply with USFDA FSMA, GMP Certification requirements for your food products. I3CGLOBAL being U...
3CGLOBAL''s team of ISO 13485 consultants and auditors who are professional and able to manage the ISO 13485 Certification process for your company. W...
FDA 510k Consultants, at I3CGLOBAL help you navigate the complete process for any medical device Class I, Class II, and Class III by thoroughly unders...
I3CGLOBAL(IN) is presenting the best services for medical device CE marking. These services are admired due to their reliability, and timely execution...
If you're also looking for a regulatory affairs specialist for your medical device then I3CGLOAL is your one-stop solution. I3CGlobal (IN) is aiming t...