Credevo is a global consulting organization supporting healthcare product development from clinical development to commercialization. Credevo provides strategic and operational support for products including - pharmaceuticals, - biologics, - nutraceuticals, and - medical devices, in areas such as ✅ Regulatory Support, ⛑ Clinical Development, 🧾 Licensing (out-/in-), and 🧑💻 Feasibility Support Credevo helps pharmaceutical / biotech / medical device companies in building clinical development strategy to accelerate product development. It works as the clinical development arm of pharma / biotech / medical device organizations, wherein they can access readily available regulatory expertise, site networks and clinical development teams. Credevo provides access to global regulatory expertise for the US, EU, Australia, China, East Asia and South East Asia regions in following areas - Marketing authorization of medicinal products - Marketing authorization of nutraceutical products - Regulatory incentives and benefits for product development for rare diseases - Approvals and permissions to initiate clinical trials With our global network of companies engaged in development of new products or those looking for new products to invest in, it becomes easier to find such attractive opportunities. Credevo also provides an extensive global feasibility mechanism to assess country-level, project-level and site-level feasibility.