Regulatory Affairs Executive
CurrentEUMDR,MDSAP, COUNTRY SPECIFIC, USFDA 510K,CDSCO
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Hetarth Patel is listed as 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, based in Unjha, Gujarat, India. AeroLeads shows a matched LinkedIn profile for Hetarth Patel.
Hetarth Patel previously worked as Regulatory Affairs Executive at Bonetech Medisys - India and Regulatory Affairs Executive at Aosys Private Limited. Hetarth Patel holds M.Pharm, Regulatory Affairs from Saurashtra University, Rajkot.
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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.
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Ahmedabad, Gujarat, India
EUMDR,MDSAP, COUNTRY SPECIFIC, USFDA 510K,CDSCO
Ahmedabad, Gujarat, India
ISO 13485, CDSCO
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Hetarth Patel works for BONETECH MEDISYS - INDIA.
Hetarth Patel is listed as 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 is based in Unjha, Gujarat, India while working with BONETECH MEDISYS - INDIA.
Hetarth Patel has worked for Bonetech Medisys - India and Aosys Private Limited.
You can use AeroLeads to view verified contact signals for Hetarth Patel at BONETECH MEDISYS - INDIA, including work email, phone, and LinkedIn data when available.
Hetarth Patel holds M.Pharm, Regulatory Affairs from Saurashtra University, Rajkot.
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