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Study Management

Site/Investigator Identification and Qualification

Central IRB Submissions

Study Monitoring
(including risk-based with biostatistics services)

Site Management

Investigational Product Management

Trial Master File Management

Study Specific Plan Development

ICF Development

Source Document Development

Vendor Management

Study Quality Risk Identification
and Management

Study Management

Site/Investigator Identification and Qualification

Central IRB Submissions

Study Monitoring
(including risk-based with biostatistics services)

Site Management

Investigational Product Management

Trial Master File Management

Study Specific Plan Development

ICF Development

Source Document Development

Vendor Management

Study Quality Risk Identification
and Management

Clinical Operations Services

With decades of experience on both the sponsor and CRO sides of drug development, our clinical operations team functions proactively by anticipating and preparing solutions for potential challenges. Our approach ensures trials progress in adherence to timelines and within budgets while always maintaining patient safety at the forefront of our strategies.

At the heart of every study.