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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

How to Navigate the APAC Regulatory Region Successfully

March 26, 2026

Read How to Navigate the APAC Regulatory Region Successfully

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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

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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

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