• 1-631-372-1052
  • 45-1 Ramsey Road, Shirley, NY 11967, USA

Early Phase Trials

Early Phase Trials

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With a global network of therapeutic experts, CD BioSciences is dedicated to providing expert CRO services for every stage of your clinical trial. All clinical trials are unique and complicated, our team is committed to helping guide our clients through the challenges of clinical trial development, partnering with our clients to shorten the whole development lifecycle, mitigate costs, as well as decrease the potential risks.

With Your Project from Day One

Early phase clinical trials (phase I and phase II trials), are the first step in evaluating the novel drugs which have been developed in the pre-clinical stage. They are critical phases to lay the groundwork for the later phase clinical trials that are yet to come. With extensive experience and clinical experts, CD BioSciences are confident to provide our clients with rigorously strategic trial design and meticulous protocol execution. Empowered by the state-of-the-art laboratory facilities and high quality staff, we are dedicated to delivering accurate and top-quality data to advance your early phase trial programs.

Stages of clinical trials.
Fig.1 Stages of clinical trials.

Full-service, Fit-for-purpose Early Phase CRO

As a flexible, reliable, committed clinical trial CRO, we provide a wide range of early phase CRO services to fit your novel drug development program. All services are executed by experts fully dedicated to the early phase program. The services include but not limited to:

  • Protocol design and early phase concept and program development
  • Protocol writing
  • Regulatory and pre-IND/IND meeting consultation services
  • Scientific consultation
  • Multi-site feasibility support based upon established QA-approved site network
  • Dedicated phase I/early development project management group
  • Phase 1 focused data management
  • Biostatistics and statistical design planning specific to early development studies
  • Pharmacokinetics
  • Clinical monitoring
  • Pharmacovigilance
  • Site management
  • Medical writing
  • Regulatory submissions
  • etc.

We offer the end-to-end clinical trial development from the start to finish. We are dedicate to executing your clinical trial to ensure the compliance with the highest standards of regulatory and scientific quality.

Our clinical trial process from start to finish.
Fig.2 Our clinical trial process from start to finish.

With state-of-the-art facilities and extensive experience in clinical pharmacology studies, we have completed various integrated clinical trials with biologics and small molecules. We have a wide range of therapeutic experts including oncology, immunology, neurology etc. to fit your unique needs of your novel drug development.

Contact Us Today for Assistance

CD BioSciences is the top ranked CRO for customer service, dedication, accountability, experts, accessibility and timely responsiveness. We are committed to be the reliable, flexible partner you can rely on to provide you with top-of-the-line services, accelerate the program progress and maximize your project's success. 

Are you looking for a professional advisor for your trials?

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