Hetarth Patel

Hetarth Patel Email and Phone Number

Medical Device Regulatory Affairs & Quality Management Representative || ISO 13485|| EU MDR || USFDA 510K || Clinical Evaluation Specialist || CDSCO Submission Expert M.PHARM (RA) @ BONETECH MEDISYS - INDIA
Hetarth Patel's Location
Unjha, Gujarat, India, India
About Hetarth Patel

Hetarth Patel is a Medical Device Regulatory Affairs & Quality Management Representative || ISO 13485|| EU MDR || USFDA 510K || Clinical Evaluation Specialist || CDSCO Submission Expert M.PHARM (RA) at BONETECH MEDISYS - INDIA.

Hetarth Patel's Current Company Details
BONETECH MEDISYS - INDIA

Bonetech Medisys - India

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Medical Device Regulatory Affairs & Quality Management Representative || ISO 13485|| EU MDR || USFDA 510K || Clinical Evaluation Specialist || CDSCO Submission Expert M.PHARM (RA)
Hetarth Patel Work Experience Details
  • Bonetech Medisys - India
    Regulatory Affairs Executive
    Bonetech Medisys - India Jun 2024 - Present
    Ahmedabad, Gujarat, India
    EUMDR,MDSAP, COUNTRY SPECIFIC, USFDA 510K,CDSCO
    View
  • Aosys Private Limited
    Regulatory Affairs Executive
    Aosys Private Limited May 2023 - Oct 2024
    Ahmedabad, Gujarat, India
    ISO 13485 , CDSCO

Hetarth Patel Education Details

Frequently Asked Questions about Hetarth Patel

What company does Hetarth Patel work for?

Hetarth Patel works for Bonetech Medisys - India

What is Hetarth Patel's role at the current company?

Hetarth Patel's current role is Medical Device Regulatory Affairs & Quality Management Representative || ISO 13485|| EU MDR || USFDA 510K || Clinical Evaluation Specialist || CDSCO Submission Expert M.PHARM (RA).

What schools did Hetarth Patel attend?

Hetarth Patel attended Saurashtra University, Rajkot, Ganpat University, S.k. Patel College Of Pharmaceutical Education & Research.

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