Site Management Organisation
SMO Services
Cavaxion provides end-to-end Site Management Organisation services to support sponsors and CROs throughout the clinical trial lifecycle — from feasibility through to closeout.
Feasibility Assessment
Rapid and accurate feasibility assessments covering patient population availability, investigator experience, site infrastructure, and competitive landscape across our network.
Study Startup
Coordination of all startup activities including ethics committee submissions, regulatory filings, site agreements, budget negotiations, and investigator training.
Regulatory Coordination
Support for CDSCO submissions, ethics committee applications, import licences, and ongoing regulatory compliance throughout the study.
Patient Recruitment Support
Targeted recruitment strategies leveraging our network's patient databases, referral pathways, and community outreach to meet enrolment targets.
Clinical Operations Support
Ongoing operational support including monitoring coordination, protocol deviation management, data query resolution, and site performance oversight.
Quality Assurance
GCP compliance oversight, internal audits, CAPA management, and quality systems support to maintain the highest standards of trial conduct.
Data Management Coordination
Coordination of data entry, query management, and EDC system support to ensure timely and accurate data collection across all sites.
Study Closeout
Comprehensive closeout support including final data reconciliation, site archiving, regulatory notifications, and closeout visit coordination.
Need SMO Support for Your Clinical Trial?
Contact our team to discuss how Cavaxion's SMO services can support your study in Andhra Pradesh.