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Kartika Puri

Kartika Puri

Regdesk Author

LinkedIn: https://www.linkedin.com/in/kartika-puri-310a6a175/


Kartika is a regulatory affairs professional with experience supporting global medical device compliance across multiple international markets, including Asia-Pacific. Kartika specializes in regulatory strategy, market entry requirements, and lifecycle management, helping organizations navigate complex and evolving regulatory frameworks with clarity and confidence.  Kartika brings a strong focus on regulatory compliance, quality, and cross functional collaboration to support successful global market access.

Articles by this author

mfds-notice 2026-6-a-detailed-comparison-of-old-vs-new-medical-device-regulatory-requirements

MFDS Notice 2026-6: A Detailed Comparison of Old vs. New Medical Device Regulatory Requirements

February 11, 2026

Read MFDS Notice 2026-6: A Detailed Comparison of Old vs. New Medical Device Regulatory Requirements

link

Uruguay Medical Device Registration in 2026: Classification, UDI, and MERCOSUR Updates

February 27, 2019

Read Uruguay Medical Device Registration in 2026: Classification, UDI, and MERCOSUR Updates

link
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