The most common problems Sponsors face when conducting clinical trials are missed recruitment targets and study delays. Choosing Nutrasource as your clinical trials partner is the first step in managing time and costs while ensuring quality research.
We specialize in early phase trials (Phase I) involving healthy volunteers, and work with clients consider the many factors involved in reaching your research goals. Studies may involve prolonged clinic visits, overnight or multi-day stays, and unique dietary controls. Whether it is using our on-site clinical research facility or one of our partners, we choose the right site for your unique objectives so that you meet recruitment targets and study goals.
At Nutrasource, we combine the right strategy, execution, resources, and tools to deliver a solution customized to your project. 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 clinical research phases by reviewing and interpreting your clinical trial data (through our data management and biostatistics services), providing you with strategic insights to aid in your decision-making.
We offer multiple early phase clinical trial solutions appropriate to your product, including:
- Adaptive clinical protocol design
- Absolute bioavailability
- Bioavailability (BA) / Bioequivalence (BE)
- Dose proportionality
- Drug-drug interaction
- Food effect
- Pharmacokinetic (PK) / Pharmacodynamic (PD)
Learn how we can help you conduct early phase clinical research to the highest degree of quality and regulatory assurance.