TCP III Certification: Market access in Taiwan

Secure a stronger position in Taiwan’s medical device market with DNV’s TCP III Certification, enabling faster, cost-effective compliance through coordinated EU–Taiwan conformity assessments.

TCP III Certification: Market access in Taiwan

DNV offers TCP III Certification, your gateway to medical device compliance and market entry in Taiwan. Under the Technical Cooperation Programme III (TCP III), DNV is officially recognized as a designated conformity assessment body, enabling seamless acceptance of audit results between Taiwan and the EU. 

Why TCP III matters 

TCP III eliminates the burden of duplicate audits by mutually recognizing inspection outcomes – saving time, reducing cost, and accelerating your entry into Taiwan’s fast-growing medical device market. 

What We Offer 

Conformity audits: Conduct approval audits to demonstrate compliance with Taiwan’s regulatory standards. 

Mutual recognition: Leverage EU-based conformity results for Taiwan approval, no need for repeat audits. 

Regulatory guidance: Help navigate complex TCP III requirements and streamline submission. 

Global support: Benefit from DNV’s worldwide technical capabilities and accredited oversight. 

Key advantages

Faster time-to-market

One audit, two markets.

Reduced costs

Avoid repeating costly on-site assessments.

Consistent compliance

Ensure alignment with both EU MDR and Taiwan medical regulations.

Why choose DNV? 

With over 160 years of assurance expertise across sectors, including medical device, DNV offers credibility, deep insight, and technical excellence. As a recognized TCP III auditor, we empower you to: 

  • Simplify compliance with coordinated EU–Taiwan audits. 
  • Leverage our global network and hands-on support. 
  • Minimize regulatory hurdles and optimize market access. 

Ready to enter Taiwan’s medical device market with confidence?

Partner with DNV to achieve TCP III Certification and streamline your market entry. Our coordinated EU–Taiwan audit approach minimizes duplication, accelerates approvals, and ensures compliance with both EU MDR and Taiwan’s regulatory requirements.