A global consulting organization supporting healthcare product development from clinical development to commercialization
Credevo provides strategic support for healthcare products including drugs, biologics, health supplements (nutraceuticals), IVD / medical devices and cosmetics in areas of Regulatory, Clinical Development, Licensing (out-/in-), and Feasibility.
A good understanding of healthcare regulations helps optimize approval timelines, increase success probabilities and accelerate product development.
Through local regulatory expertise worldwide, Credevo facilitates
Do you know it's possible to improve the clinical trial performance significantly with simple yet powerful steps?
Credevo's expertise in clinical development achieves just that and accelerates clinical trials with
Building a foresight before investing time and money in a project helps achieve faster identification of challenges and possible solutions.
With innovative tools, international strategic teams and information network, Credevo facilitates feasibility assessments for
Development of great products often needs a collaborative effort. Credevo’s licensing support is about connecting with excellent products, developers, investors, and marketers worldwide.
Utilizing a global network of companies, Credevo assists in out-licensing and in-licensing of healthcare products and assets worldwide.
Looking to develop novel products, explore new markets, or accelerate your clinical trials? Start with feasibility assessments for your products, new markets or clinical trials sites. Explore Now!
Like your clinical trials to be faster, more efficient and of higher quality? Let's work together to develop an effective strategy, identify ways to accelerate and work with experts. Start Now!
Struggling with regulatory hurdles and ambiguities in one or more countries? Utilize regulatory specialists having expertise specific to your product and target country. Try Now!
Utilize our special focus on North America and Asia-Pac regions.