Information for Research Sponsors
An experienced, multidisciplinary research team
Pulse Heart Institute provides comprehensive clinical trial infrastructure to numerous investigators. Our researchers are clinicians with deep expertise and national renown who participate in and are closely aligned with our system-wide Centers of Excellence.
Our dedicated research administrative team ensures expedient startup and quality data for our community research partners and industry sponsors. Our capabilities include:
- Good Clinical Practice (GCP) and Human Subject Protection (HSP) trained investigators and dedicated research staff, as well as routine GCP and HSP training for all staff and investigators
- Ability to process pK samples
- Ability to use central IRB of sponsor’s choice
- Dedicated study monitoring space
- E-regulatory system
- In-house secure pharmacies
- Integrated data sharing and report building with Epic electronic medical records
- Internal quality assurance program
- Local full-service CLIA-certified laboratories
- Study startup averaging 75-90 days, including regulatory, budget and contract activities
If you’re seeking sites to conduct a clinical trial of any kind (Phase I–V, observational, device, registry, etc.), please contact the Pulse Research Team.