A global consulting organization, headquartered in Singapore, supporting healthcare product development from clinical development to commercialization
Credevo offers comprehensive clinical trial support, from strategy to execution, including end-to-end clinical trial services in Asia-Pac and North America. These include full range of services for clinical trial management and specialized bioavailability/bioequivalence studies.
With a reach to more than 150,000 investigators worldside, Credevo facilitates super quick site identification and clinical trial feasibility.
Credevo also provides market access support through business development, regulatory support, and licensing services, covering regions such as Southeast Asia (Singapore, Vietnam, Thailand etc), East Asia (South Korea, Japan), and Pacific region (Australia, New Zealand) facilitating smooth healthcare product development and commercialization.
Utilize a fully integrated approach to clinical trials, guiding you from strategic planning to thorough execution, with quality at the core of every step
"Greatly appreciate Credevo's fast and diligent services in clinical development strategy and feasibility support in Asia-Pac that helped us with our strategic planning in the territory. We highly recommend Credevo for their clinical development services."
Tim Keutzer, COO @Spero Therapeutics
Credevo offers in-depth clinical trial feasibility assessments to identify investigators and sites, estimate project recruitment rate, assess design, pre-empt timelines and costs.
With access to more than 150,000 investigators globally, innovative tools, international strategic teams and information network, Credevo facilitates clinical trial feasibility and site identification across Asia-Pac, North America and other regions.
"Thank you very much for a great support with feasibility assessment and timely delivery"
Mr. GS, Feasibility Recruitment and Site Engagement Lead-APAC @Multinational CRO from Australia
A good understanding of healthcare regulations helps optimize approval timelines, increase success probabilities and accelerate product development.
Through local regulatory expertise worldwide, Credevo facilitates
"Highly appreciate and thankful for the support with regulatory submission and clinical trial assessment in Australia for our product"
Mr. Chung, Managing Director @BrainOn Inc, South Korea
Click on the flag to know more
Talk to us for Clinical Trials in North America and Asia-Pac