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4 candidates for "Medical Devices"
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Aparna Kumar

Medical Devices
Pune
Seasoned professional specializing in Medical Device Regulation (MDR) remediation and ISO 13485–aligned Quality Management Systems (QMS). Experienced in compliance, audits, and continuous improvement to enhance…
EUMDR ISO 14971 ISO13485 Quality Assurance Regulatory Affairs (RA)

Manasa R

Medical Devices
Pune
Medical Electronics background from Dr. Ambedkar Institute of Technology Works at Tata Elxsi in regulatory affairs (APAC region) Prepares Global Submission Summary Documents (GSSD) &…
Regulatory Affairs (RA) Regulatory Analysis Regulatory submissions

sonia sharma

Medical Devices
Mumbai
Regulatory Affairs Executive - QMS || ISO 13485 || Technical Document preparation|| GSPR || 510k USFDA Medical Device || EU MDR ||SFDA (GHAD )& CDSCO…
Regulatory Affairs (RA) Regulatory Analysis Regulatory Compliance

Naveen Kumar S

Medical Devices
Pune
Senior engineer | Regulatory Affairs | EU MDR 2017/745 | ISO 13485 | ISO 14971 l Loftware | DHF remediation | Labeling | Kallick |…
Regulatory Affairs (RA) Regulatory Compliance