CGI has extensive experience working with clinical trial sponsors and CROs to understand their regulatory information management.

Why do you need to effectively manage your TMF? Trial Master File (TMF) is the common term for a sponsor’s regulatory-required ...

Whether you’re a clinical trial manager, regulatory affairs professional, or clinical pharmacist, your work is a vital contribution.

A part of a greater whole that provides life-saving therapies for patients.

Therapies that improve the lives of populations.  Programs that improve the cost and affordability of care. Strategies that help your organization improve patient experiences and drive engagement.

At CGI, we understand your mission and we’re here to help.

We’re a proven partner for empowering patient-centered digital innovation and business transformation in health and life sciences.