• Spotting of appropriate candidate sites & best qualified investigator(s) for counseled clinical studies.
  • Provision of administrative logistics to study executing body (drug company or CRO), bilingual translation of protocols, agreements and reports as per the need of involved parties.

CRO conducted studies support:

  • Selection of sites, securing needed protocol approvals, handling Ministry of Health (MOH) relevant logistic procedures, and adequate translation to local language.
  • Monitor/follow up of company sourced Phase II / Phase III clinical studies.
  • Conducting Phase IV marketing oriented clinical trials (PMS).
  • Coordination of Regional and International multi-center studies conducted at institutions within Quadri territories.

Medical Support