Organization for global clinical development and healthcare product registration worldwide.
Credevo is a global clinical research and development company that provides strategic support for clinical development and product registrations worldwide.
Through innovative online platform, Credevo facilitates clinical trial feasibility with more than 100,000 investigators around the world.
With a network of local regulatory expertise around the globe, Credevo supports regulatory submissions, approval process and development of regulatory strategies for all major regions.
Credevo provides access to thousands of clinical trial sites, investigators, regulatory specialists and other services providers across regions globally.
Credevo provides you with strategic consultancy, regulatory support, clinical trial feasibility, market intelligence and operation support for clinical development projects and product registrations worldwide.
Strong awareness of regulatory requirements helps ease the product development process, clinical trials planning as well as product approval.
Do you know with such clarity, it’s also possible to optimize approval timelines, success probabilities and accelerate development?
Do you know that performance in most of the clinical trials can be improved significantly with simple, yet powerful steps?
Do you know that choice of region, trial sites and trial teams can impact more that 90% of your metrics?
Performance of clinical trial sites exponentially impacts the trial metrics. A trial successfully executed can lead to market domination for your product.
Why to lose this opportunity? Start by choosing the sites that recruit faster, provide quality and vastly improve your trial performance.
Do you prefer your clinical development to be strategically faster, more efficient and of higher quality? Develop your clinical development strategy, devise project plans and build teams with experts.Start Now
Are you looking for investigators in a new region, therapeutic segment or just another new trial? Reach thousands of investigators and perform feasibility online with interested investigators.Find 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