Blog Posts

Learn how to prepare a compliant dossier for Vietnam medical device registration in this guide for foreign manufacturers.

Explore Vietnam’s fast-track and standard medical device registration pathways and the role of reference approvals in shortening timelines.

Discover how leveraging Real World Data generated in the Greater Bay Area can accelerate market entry for medical products in China.

Learn the key requirements for China food labeling compliance: mandatory label content, ingredient declarations, imported food requirements, and more.

Identify China medical device GMP gaps and prepare QMS, supplier, data, and inspection controls before NMPA market entry.

Learn how China IVD risk classification works under NMPA rules and see common compliance pitfalls to avoid.

Learn about China's Unique Device Identification (UDI) system and how to navigate China’s evolving medical device market.