Our

Capabilities

What we offer

eSource and eRegulatory

With real-time data collection and entry of electronic source data during participant visits, we:

  • reduce human transcription errors

  • reduce protocol deviations

  • streamline monitor vists making them more efficient

  • provide easy access for data/document monitoring through the secure cloud host

  • ensure ALCOA+ standards are met

  • ensure the reliability, quality, integrity, and traceability of data

Fast Study Startup

  • Quickly and efficiently negotiate study budget and contracts

  • Utilize central IRBs

  • Utilize CTMS for study invoicing and payments

Participant Network

We have developed trusted relationships with physicians, community clinics and nonprofits that serve historically underrepresented communities to rapidly engage a diverse cohort of participants.

Quality Assurance

We’ve developed a robust internal QA program to identify and prevent noncompliance with protocol, FDA regulations and ICH GCP.