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Clinical Trial Planning


Creating a successful clinical strategy must focus on quality at every stage. From choosing trial endpoints and inclusion/exclusion criteria, to data analysis and final report completion, we pay attention to trial goals from the start.

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.

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