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ICON plc
About CRO
Global full-service CRO providing outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device industries.
Technology & Expertise
We have built ICON plc's capabilities around Clinical Operations & Trial Management, Data Management & Biostatistics, Regulatory Affairs & Submissions, Drug Safety & Pharmacovigilance. That expertise includes feasibility, project management, site coordination, and study close-out; data standards, cleaning, analysis plans, tables, listings, and figures; planning and delivery of regulatory documents across development milestones; and connected specialist capabilities, supported by program-specific methods, resources, and delivery planning.
Core Services
At ICON plc, we deliver Clinical Operations & Trial Management, Data Management & Biostatistics, Regulatory Affairs & Submissions, Drug Safety & Pharmacovigilance through flexible engagement models. Services may bring together study start-up, cross-functional trial oversight, and operational delivery; clinical database design, data review, statistical programming, and analysis; regulatory strategy, dossier development, submission management, and authority support; and connected specialist capabilities, allowing teams to expand or narrow support as a program evolves.
Accreditations & Compliance
ICON plc manages compliance according to the regulations, methods, and locations relevant to each engagement. Facility credentials and certification scope are confirmed during qualification rather than assumed across the organization.
