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Experts Share Insights on Evolving Global Vaccine Landscape Including mRNA Trends

Experts Share Insights on Evolving Global Vaccine Landscape Including mRNA TrendsSINGAPORE, March 03, 2023 (GLOBE NEWSWIRE) Novotech, the leading Asia Pacific centred biotech CRO with extensive experience in vaccine trials, is convening an expert panel webinar with Endpoints News covering the evolving landscape i.

Experts Share Insights on Evolving Global Vaccine Landscape

Investegate |Novotech Announcements | Novotech: The Evolving Global Landscape in Vaccine Development: Novotech and Endpoints News Webinar

The Asia-Pacific Region A Hot Spot For Clinical Trials

The Asia-Pacific Region: A Hot Spot For Clinical Trials By Mathini Ilancheran, principal analyst, R&D, Beroe Inc. Introduction The Asia-Pacific region has become the hot spot for conducting clinical trials due to the ease of regulatory compliance, the low cost of conducting studies, a growing patient population, and the presence of a few top clinical institutions acting as sites. For example, the regulatory agencies in China are working toward an enhanced clinical trial process by reducing the overall review and approval process. 1 The clinical trial workforce contributes to around 30 to 35% of the overall trial cost. This makes FTE rates for clinical research a key parameter to consider. These rates are generally higher in the developed markets as compared to the Asia-Pacific region, which is why the latter is becoming an important location for conducting clinical trial studies. Also, the cost per patient across all therapeutic areas and phases is much lower in Asian countries

The Asia-Pacific Region A Hot Spot For Clinical Trials

The Asia-Pacific Region: A Hot Spot For Clinical Trials By Mathini Ilancheran, principal analyst, R&D, Beroe Inc. Introduction The Asia-Pacific region has become the hot spot for conducting clinical trials due to the ease of regulatory compliance, the low cost of conducting studies, a growing patient population, and the presence of a few top clinical institutions acting as sites. For example, the regulatory agencies in China are working toward an enhanced clinical trial process by reducing the overall review and approval process. 1 The clinical trial workforce contributes to around 30 to 35% of the overall trial cost. This makes FTE rates for clinical research a key parameter to consider. These rates are generally higher in the developed markets as compared to the Asia-Pacific region, which is why the latter is becoming an important location for conducting clinical trial studies. Also, the cost per patient across all therapeutic areas and phases is much lower in Asian countries

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