Dear
Colleagues,
Among
emerging Asian markets, South
Korea is quickly becoming a dominant
outsourcing location for clinical trials. This is mostly due to a quickly
evolving regulatory environment, streamlined regulatory approval, reduced costs, and more successful patient
recruitment relative to many developed Western countries.
We have
recently published an article in the May issue of the International Clinical
Trials magazine entitled "Korea Path" (pp 30-36) which discusses the country's
current clinical research environment, including the challenges that must be
addressed by foreign companies.
What are the translation requirements? How do
cultural differences affect medical practices? What is the current regulatory
approval process?
We hope
you take this opportunity to read the article, and that it provides you with
new and useful information.
Please also check out our other recent publications to learn more about global clinical trials and biomanufacturing.
As a
language service provider for over fifteen years, we are well aware of the
importance of native language communication, especially in the translation of
clinical trial documents. Our life science experts have translation experience
in over one hundred languages, including Korean, and other
dominant Asian languages.
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