Industrial Development Administration, Ministry of Economic Affairs
Medical Device Industry Innovation Transformation & Market Expansion Program
醫材產業創新轉型與市場拓展計畫
Eligibility
Legally registered manufacturers whose products meet Taiwan-origin certification requirements.
What’s offered
Three tracks: technology counseling to clear technical bottlenecks for cross-domain device development and speed clinical introduction; cross-domain validation that supports joint innovation and clinical-effectiveness studies; and international market-entry support, including regulatory document preparation and validation for foreign markets.
Key terms
- Cost share
- 1:1 government / company match.
- Application
- Submit the electronic project document with unit-signature pages.
- Notification
- Feasibility evaluation, joint plan drafting, then submission to IDA / MOEA for review.
Application process
- 1Submit application
- 2Eligibility review
- 3Presentation review
- 4Contract signing
- 5Begin counseling
Program structure
Tech counseling / cross-domain cooperation / market validation / industry transformation
- Technology counseling — Overcome cross-domain product technology bottlenecks; accelerate clinical introduction and on-site adoption.
- Cross-domain validation — Joint innovation R&D between firms, including pre-clinical R&D, applied research effectiveness, and clinical-effectiveness validation.
- International market entry — Complete regulatory document preparation for foreign markets, plus validation work to seize commercial opportunities.
Application window
Per official announcement each cycle.
Who to contact
Industrial Technology Research Institute (ITRI)
財團法人人工智慧技術研究院
Mr. Hsu (許先生)
English-language application support: not confirmed. Plan to bring a Mandarin-fluent collaborator to the first conversation.