Pharmacology Studies

AXIS is your preferred partner for all your pharmacology studies

We are a leading clinical pharmacology CRO, well-equipped to accelerate the progression of your clinical development plan in clinical research.

We are accomplished at all early-stage studies required for drug development

  • First-in-Human
  • Bioavailability / Bioequivalence
  • Pharmacodynamics
  • hADME
  • Drug-Drug Interactions
  • Linearity and Dose Proportionality
  • Single and Multiple Ascending Dose
  • Food Effect
  • High Precision TQT, Cardiac safety
  • Dermal Open Flow Microperfusion

Our onsite bioanalytical laboratory provides expedited analysis as part of our integrated clinical pharmacology services, especially in dose-escalation pharmacology studies.

We have optimized the science of recruitment for healthy volunteers and specialty populations

Our recruitment and marketing team has streamlined the process for rapid recruitment, supporting our role as a specialized CRO in clinical research for pharmacology studies.

Expansive Database

With our database of more than 20,000 volunteers at our Minnesota center, we have the capability to recruit for multiple studies every month.

Geographic Benefit

Proximity to five universities and colleges provides us access to a large population of healthy volunteers.

Community Involvement

We participate in many local community and university events to promote recruitment for your study.

Our integrated eSource and EDC system ensures quality and consistent data

  • We collect study data at our Phase I center in Minnesota electronically in ClinSpark®, the industry-leading eSource/EDC solution for Phase I studies.
  • The eSource system integrates seamlessly with medical devices such as electrocardiograms, vitals monitors, and scales/stadiometers, allowing for real-time data collection and preventing data entry errors.
  • Bi-directional data connectivity with our clinical safety lab using Health Level 7 and Laboratory Data Model standards established by CDISC ensure real-time safety monitoring.

Our pharmacists will aid you in the development of a robust drug preparation, compounding, and dosing protocol and provide training to ensure consistent dosing.

Our integrated eSource and EDC system ensures quality and consistent data

  • We develop a customized approach to manage each project
  • We start with a structured kick-off meeting to ensure that every project is carefully planned for timely communication and a seamless workflow
  • We conduct each study with the highest quality and precision to meet regulatory approval

Our team’s highest priority is to achieve satisfaction of each of your stakeholders through project engagement to successfully execute the study.

Interested in bringing your study to AXIS? Please reach out:

John Pottier
Senior VP Business Development