Kaderasan M
Medical device Regulatory affairs/USFDA 510k/EUMDR/Submission/Risk management / DHF remediation / Labelling / Technical documentation/ 21 CFR 820 /ISO13485, ISO14971/ISO 15223-1/EN ISO 20417/IEC 62304/IEC 60601-1.
- Role
- Specialist at L&T Technology Services
- Location
- Bengaluru, KA, IN
- LinkedIn followers
- 500 followers
About Kaderasan M
Demonstrates extensive expertise in Medical device Regulatory affairs, including…
Experience
Specialist
Apr 2025 — Present · Bengaluru, IN
To provide strategic insights and operational support to the Regulatory Affairs team by leveraging data analytics to monitor, evaluate, and report on 510(k) submissions, team performance, and regulatory trends. This work supports informed decision-making, competitive benchmarking, and continuous improvement in regulatory compliance and submission efficiency.Enhances visibility into regulatory performance and market trends.Supports strategic planning and competitive analysis.Improves team efficiency and submission quality.Enables data-driven decision-making for future regulatory strategies.Driving Operational EfficiencySupporting Cross-Functional Collaboration
Education
Tamilnadu college of engineering-cbe
BE, automobile engineering
2008 — 2012
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