Rajesh Duppelli
Biomedical Engineer | Regulatory Affairs Specialist | EU MDR, FDA 510(k), CDSCO & TFDA | ISO 13485 & 14971 | CSRD Sustainability
- Role
- Regulatory Affairs Specialist at Wipro
- Location
- Hyderabad, TG, IN
- LinkedIn followers
- 500 followers
About Rajesh Duppelli
I\'m Biomedical Engineering with skill in the field of Medical Devices Regulation and Medical Equipment Maintenance.Regulation affairs knowledge Gap analysis TFDA (Taiwan regulation). UDI-DI submission / PIE (Product industrialization engineer support) EUMDR/ MDD to MDR Transition/ NPI 13485:2016 QMS and 14971 Risk Management certified.CSRD SUSTAINABLETY EU region Philips
Experience
Regulatory Affairs Specialist
Feb 2026 — Present
Education
Vishwa shanthi high school
SSc
Govt institute of electronic
Diploma of Education, Biomedical/Medical Engineering
Osmania University
Master of Technology - MTech, Electronic and Biomedical Engineer
Osmania University
Master of Engineering - MEng, Biomedical/Medical Engineering
University college of Engineering,Kothagudam
Electronic and communication engineering , ECE
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