About Us

About Us

About Us

Extensive Experience

Located in the USA, CD BioSciences provides a full range of clinical trial consulting, design, conduction, management, reporting and analysis services to advance your clinical trial development. CD BioSciences continuously provides professional support to local, national and international clients. Our clinical trial services focus on the entire clinical trial lifecycle, including bioanalytical lab testing, clinical pharmacology, first-in-human (FIH), proof of concept (POC), early phase trials, phase IIa trials, phase IIb-III trials, phase IIIb-IV trials, CDM analysis and reporting. We guarantee the confidentiality and sensitivity of our customers’ data.

Quality First

Quality is the cornerstone of CD BioSciences’ success. The primary task of CD BioSciences is to guarantee work quality and to comply with regulatory requirements. Our highly trained staff will strictly implement quality control procedures and deliver work results on time without compromising quality. In order to maintain strict quality control standards, we do not subcontract services. We adhere to the transparency of all clinical and business processes.

Our Goals

With innovative perspectives on the design and analysis of clinical trials and other studies, CD BioSciences is intended to save the client's time and cost from development to market. And we will deliver our clients with high quality databases, comprehensive statistical reports and final statistical files used for regulatory submission to advance the progress of pharmaceutical industry or accelerate their studies. We believe the establishment of a customer-centric business model will become the key point to accelerate the drug development process, share accessible resources and gather a team from different backgrounds to conduct clinical trial projects in the future.

Why Choose Us

CD BioSciences provides you with one-stop service to accelerate your project development.

Are you looking for a professional advisor for your trials?