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Caidya
About CRO
Asia-focused CRO providing clinical trial management, regulatory strategy, and biostatistics services for multinational and domestic pharmaceutical companies.
Technology & Expertise
At Caidya, our technical expertise covers Clinical Operations & Trial Management, Regulatory Affairs & Submissions, Data Management & Biostatistics. We combine study start-up, cross-functional trial oversight, and operational delivery; regulatory strategy, dossier development, submission management, and authority support; clinical database design, data review, statistical programming, and analysis to build practical workflows around each program's scientific objectives and development stage.
Core Services
Caidya's core offering covers Clinical Operations & Trial Management, Regulatory Affairs & Submissions, Data Management & Biostatistics. We organize feasibility, project management, site coordination, and study close-out; planning and delivery of regulatory documents across development milestones; data standards, cleaning, analysis plans, tables, listings, and figures around program goals so that responsibilities, outputs, schedules, and handoffs are clear from the outset.
Accreditations & Compliance
Quality and compliance at Caidya are evaluated at the service and facility level. We recommend reviewing current certificates, inspection history, quality-system scope, and any study-specific requirements before work begins.
