Ankita Tandulje, Author at Artixio

Author name: Ankita Tandulje

Ankita Tandulje, a Regulatory Affairs Professional, has strong expertise in navigating regulatory frameworks and providing effective regulatory strategies for product approvals and lifecycle maintenance across global markets. Through practical experience in documentation, dossier preparation, and submission, she offers insights that help readers to interpret complex regulatory requirements and align with evolving global standards, supporting compliance and strategic regulatory planning.

HSA Singapore Investigational Product Management Guidance

Ankita Tandulje / February 23, 2026 / HSA Compliance, Regulatory Updates

For locally registered products in Singapore, the management of investigational product (IP) for clinical trials is the most critical step, […]

Mexico COFEPRIS 2025: Medical Device Registration Update

COFEPRIS Compliance, Regulations, Regulatory Updates

COFEPRIS Simplifies Medical Device Registration in Mexico (2025)

Ankita Tandulje / February 16, 2026 / COFEPRIS Compliance, Regulations, Regulatory Updates

New Regulatory Agreement by COFEPRIS for Simplification of Medical Device Registration Procedures and Shorter Timelines in Mexico: The Federal Committee