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Powering business transformation

We’re your partner in ensuring your organization’s clinical and regulatory operations are effective, monitored and inspection ready. With a focus on both business and technology, CGI delivers an innovative, strategic approach to support the entire life cycle of product development.

From the lab to manufacturing, our expertise spans the entire product development process. We ensure your product development and value chain leverage the right technology at the right time for the proper business use—from study planning and clinical study reporting to regulatory submission and approval.

700+
Biotech and pharmaceutical projects completed for over 50 clients
95%
Repeat engagements with life sciences clients
9.47
Out of 10 average global client satisfaction scores in life sciences
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A sampling of our domain expertise

Clinical trials and content management
Commercial operations

Market dynamics are shifting. Your organization must relinquish traditional operations for a more fit-for-purpose digitized model. This means leveraging the right digital infrastructure and tools to deliver strategic imperatives including maintaining the competitive edge, delivering value-based outcomes for patients, and making treatments more affordable and accessible. We help you put innovative therapies in the hands of people who need them.

Regulatory information and operations

As your regulatory partner, we leverage our regulatory information management (RIM) strategy and road mapping expertise to optimize operations across your organization. Our framework addresses your RIM vision's people, process, information, and technology aspects and ensures alignment among executive and business leaders.

Quality and manufacturing services

CGI empowers quality, manufacturing and compliance teams to realize competitive advantages throughout the value chain while minimizing risk exposure, increasing efficiency and safety standards, and reducing costs and time to market.