Taiwan

With a strong growth market for drug development, dense population, and a universal healthcare system, Taiwan is an ideal location for clinical trials.

Taiwan is one of Emerald Clinical’s fastest‑growing Asian hubs. With a strong growth market for drug development, a dense population, and a universal healthcare system, Taiwan is an ideal location for clinical trials. Emerald Clinical’s on‑the‑ground clinical team leader oversees a number of our CRAs and CTAs in delivering customer projects across Taiwan. The Center for Drug Evaluation (CDE) was established by the Ministry of Health and Welfare (MOHW) to assist the Taiwan Food and Drug Administration (TFDA) in the technical review of new drugs, medical devices and clinical trials to fulfill regulatory requirements.

The MOHW regularly accredits sites for clinical trial conduct, where the certificate is valid for four years. There are 128 qualified sites for conducting clinical trials in Taiwan. Known centers for excellence include the National Taiwan University Hospital, which currently runs more than 600 clinical trials, including 43 Phase I clinical trials; and Chang Gung Memorial Hospital, which currently runs more than 500 clinical trials. There is strong government support for clinical trials.

What are the benefits of conducting clinical trials in Taiwan?

  • Taiwan is a strong growth market for drug development
  • Approximately 80% of trials in Taiwan are multinational trials
  • Almost 100% of Taiwanese nations are covered by the National Health Insurance (NHI) program, which provides universal quality healthcare to its population at an affordable cost
  • Clinical Trial Notification and c‑IRB Mechanisms provide a fast study start‑up timeline

Why is Emerald Clinical the CRO of choice for our sponsors in Taiwan?

  • Experienced team managing Phase I to IV clinical trials.
  • Established network
Taiwan: Level 57, Taipei 101 Tower, No.7, Section 5, Xinyi Road, Taipei City, 110, Taiwan