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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

RIM Software for Scaling Medtech: How to Add Markets and Products Without Adding Headcount

August 24, 2026

Read RIM Software for Scaling Medtech: How to Add Markets and Products Without Adding Headcount

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How to Manage Regulatory Change Impact Across Markets Without Missing a Renewal

August 11, 2026

Read How to Manage Regulatory Change Impact Across Markets Without Missing a Renewal

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Regulatory Submission Tracking Software: What to Look For in a Modern Platform

Regulatory Submission Tracking Software: What to Look For in a Modern Platform

August 5, 2026

Read Regulatory Submission Tracking Software: What to Look For in a Modern Platform

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Regulatory submission

Regulatory Submission 101: How Global MedTech Teams Manage Multi-Market Filings

July 31, 2026

Read Regulatory Submission 101: How Global MedTech Teams Manage Multi-Market Filings

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RIM Software for Medical Devices

RIM Software for Medical Devices: What Sets RegDesk Apart from Legacy Platforms

July 24, 2026

Read RIM Software for Medical Devices: What Sets RegDesk Apart from Legacy Platforms

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How to stop manually checking Regulator website

How to Stop Manually Checking Regulator Websites (Without Missing Important Regulatory Changes)

July 20, 2026

Read How to Stop Manually Checking Regulator Websites (Without Missing Important Regulatory Changes)

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APAC

Medical Device Registration in APAC: The Complete Reference Guide

May 11, 2026

Read Medical Device Registration in APAC: The Complete Reference Guide

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How AI Is Transforming Regulatory Intelligence for Medical Devices

May 4, 2026

Read How AI Is Transforming Regulatory Intelligence for Medical Devices

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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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