Development of clinical protocol , Phase I to IV and RWE

Design, development, of CRFs and eCRFs platform

Monitoring

ICF development in compliance to international and country regulations

Selection of sites, staff training

 Close interaction and selection of vendors/partners such as central lab, image lab, IVRS, etc

Development of study related materials to sites, pharmacy manual, advertisement materials etc

Investigator Meeting organization

Technical translations

Creation and submission of regulatory packages and dossiers for Regulatory approvals

Regulatory Ethics approval and follow-up during the whole study duration

Medical Support , case management, SAEs, SUSARs, hotline 24/7

Development of database and statistical services