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Online event

Navigating Taiwan's healthcare market: Regulatory pathways for UK exporters

Wednesday 11 November at 9:00AM

Get a practical introduction to Taiwan's healthcare regulatory landscape and market entry process.

What you’ll learn

  • Gain an understanding of Taiwan's regulatory and market access environment for pharmaceuticals and medical devices.
  • Identify key considerations and common challenges when introducing healthcare products into Taiwan.
  • Learn practical strategies to support successful market entry and commercial growth in Taiwan's healthcare sector.

Description

Taiwan offers significant opportunities for UK life sciences, pharmaceutical and medical device companies, supported by a sophisticated healthcare system, strong demand for innovative healthcare solutions, and growing UK-Taiwan trade links. Notably, pharmaceutical products remain the UK's largest goods export category to Taiwan, highlighting the strength of commercial engagement between the two markets. Besides, in 2026, Taiwan once again ranks No. 1 in the Health Care Index by Country, maintaining its leading position globally for consecutive years.

Delivered in partnership with RAPS Taiwan, this webinar will provide UK exporters with a practical introduction to Taiwan's healthcare regulatory landscape and market entry process. Participants will gain insights into regulatory requirements for pharmaceuticals and medical devices, market access considerations, product registration pathways, healthcare reimbursement, and key factors for successful market entry.

The session is designed for UK businesses exploring opportunities in Taiwan or seeking to expand their presence in the market, helping them better understand the regulatory environment and identify routes to commercial success in one of Asia's most advanced healthcare markets.

Speakers

Pei-Ting Sarah Chou

Supervisor & Consultant/Founding Board of Director, RAPS Taiwan

As a U.S./Taiwan certified regulatory professional and ISO13485/ISO9001 lead auditor with European regulatory trainings funded by British Council and DAAD, the speaker serves as the founding Board of Director and the current Supervisor and Consultant at Regulatory Affairs Professionals Society (RAPS) Taiwan Chapter. The speaker has led the teams at North American, European & Taiwanese firms to pass manufacturing line/certification audits conducted by health authorities around the globe. Having delivered health authority training programs, the speaker has played the roles as a contributor of ISO conference roundtable, an Advanced Medical Device Advisory Seed Member of Taiwan FDA, an AHWP Technical Committee Member, a reviewer of International Production Journal, a lecturer/trainer of the APEC Medical Devices Regulatory Science Center of Excellence Workshop, a Medical Center Mentor, a BCCT Mentorship Program Mentor and a RAPS published book author.

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