- 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.