Early Phase Clinical Trials

Missed recruitment targets and study delays are the most common problems faced in clinical research.  Choosing Nutrasource is the first step in managing time and costs while ensuring quality research.  We have a speciality in early phase trials involving healthy volunteers.  Early phase trials may have many factors that must be considered to achieve the research goals.  Studies may involve prolonged clinic visits, over night or multi-day stays, and unique dietary control.  Whether it is using our on-site clinical research facility or one of our partners, we choose the right site for your specific goals to achieve study goals and ensure recruitment targets are met.

We combine the right strategy, execution, resources and tools to deliver a solution unique to your goals.  Experienced in first-in-human and healthy subject trials as well as later stage efficacy studies, we can help you transition your product through the phases of clinical research by reviewing and interpreting your clinical research data and provide you with unique insights for decisions.

At Nutrasource, we understand that product development isn’t one-size-fits-all.  In order to provide you with the service appropriate to your product, we offer multiple early phase solutions, including:

  • Adaptive clinical protocol design  
  • Absolute bioavailability
  • Bioavailability (BA) / Bioequivalence (BE)
  • Dose proportionality
  • Drug-drug interaction
  • Food effect
  • Pharmacokinetic (PK) / Pharmacodynamic (PD)
  • Sleep

Looking for more information on early phase clinical trials? Contact a member of our team today or email us directly at info@nutrasource.ca. You may also request a customized quote and we will contact you with details within two business days.