Clinical Trial Planning
IRB/EC/REB Regulatory Submissions
The Global team can assist with the regulatory strategy development, provide services for local and national regulatory agency submissions and keep you in compliance with reporting requirements for each geography.
Site Selection, Qualification, and Initiation
GLOBAL CRO leverages a robust network of investigators. Our clinical team brings strong relationships that have been built over years working in the medical device and pharmaceutical industries in multiple therapeutic areas.
Vendor Selection and Management
GLOBAL CRO has an extensive network of vendors we have worked with on multiple trials. By starting with a narrowed list, you can streamline the vendor selection process and potentially reduce costs.
Our experienced biostatisticians integrate into our clinical trial teams, seamlessly providing the necessary support to ensure your trial is supported with adequate sample size and achievable endpoints.
Contract and Budget Negotiations
Our clinical trial agreement template has been created from years of experience with negotiations from private clinics to large hospital conglomerates and can be customized to include your company’s specific requirements.