Clinical
Sites

Our research sites are outfitted with cutting-edge facilities and staffed by seasoned clinical teams committed to executing trials with precision and in strict accordance with the highest industry standards Everywhere we are present.

CRU Global conducts clinical trials within its dedicated early-phase units, Phase 1 units, and later-phase inpatient and outpatient clinics. To accommodate the growing number of study requests and the need for specialized patient populations, CRU Global has established and manages several partner sites, as well as preferred partnerships with select facilities.

Our partner sites include renowned and experienced university clinics, university hospitals, national institutes, and hospitals, all of which are home to numerous Key Opinion Leaders.

Phase I-IV Clinical Trials

Country feasibility, site and investigator selections are crucial steps for any clinical trials, as it impacts the study for its whole duration.

Early Development
Trials

  • Phase I – II Proof-of-Concept [POC]
  • Adaptive design studies: healthy volunteer & patient
  • First in Human [FIH]
  • Single Ascending Dose [SAD]
  • Multiple Ascending Dose [MAD]
  • Bioavailability/ Bioequivalence [BA/BE]
  • Pharmacokinetics/ Pharmacodynamics [PK/PD]
  • Dose ranging and Tolerability studies
  • Food Effect studies
  • Drug-Drug Interaction studies

Partner Sites

For rare diseases, niche indications, or fast-track recruitment, CRU-GLOBAL activates top-tier partner sites—leading academic centers and university clinics with KOL investigators. These sites, affiliated with local CRU offices, offer high recruitment potential, and studies are fully or partly managed by CRU to ensure appropriate oversight, quality and speed in delivery.

CRUINT GLOBAL Consulting Pte. Ltd.

Thank you for reaching out to CRU Global. If you have any questions or would like more information about our services, please don’t hesitate to contact us using the details below.