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Clinical Solutions

Drive creative problem-solving with our diverse and experienced team in clinical development, technology and patient access solutions.

Manage the complexity of Phase I trials

Keep moving forward with confidence through critical go/no-go decisions and first-in-human (FiH) trials. We operate our own state-of-the-art clinics and augment them with a global network of specialist sites. Let us navigate the complexities of early phase studies and deliver unique insights that inform your critical decisions.

First in Human

Consulting for every phase of your product journey

Enable a more efficient development process. Our regulatory strategy, product development and market access and HEOR consulting teams align with your clinical and commercial goals, providing agility and flexibility throughout the entire continuum of your product development. 

Consulting

Upgrade your site experience 

We’re leading the way in transforming the landscape of clinical research by listening, collaborating and responding to the needs of sites, leaving them free to do what sites do best—patient care. Learn how our streamlined, integrated clinical trial experience benefits patients, sites and trials.

Site Connections

End-to-end safety solutions

Maintain patient safety from trial startup to post-market with our integrated pharmacovigilance services. Patient safety is our number one priority, and with over three decades of experience, our experts know how to get it right—the first time.

Safety

Advance your clinical development

Proactively tackle challenges with our robust clinical development solutions, enabling faster decision-making and exceptional customer experiences. Working closely with you, we help minimize patient burden, improve access and deliver real-time results to inform your decision-making.

임상 개발

Adaptive delivery models 

Rapidly adapt to evolving needs with our dynamic delivery models. Insource or outsource the skills and capabilities you require. We ensure your clinical development stays agile, efficient and aligned with your strategic goals from start to finish.

Delivery Models

It’s a privilege to be working with each one of you. Amazing team and amazing accomplishments!!! Simply put—Fortrea is an incredible team who has stepped up each time to deliver over and over again.”

Director PV Automation

Fortrea is an incredible team who has stepped up each time.

Med tech—done right

Bring your medical device or diagnostic product to market with confidence. Our dedicated med tech team, invested in key certification standards such as ISO 13485, ensures the highest standards of quality and safety to support everything for your in vitro diagnostic.

의학 기술

RWE & post-approval studies

We have the experience and know-how to help sustain your product’s success post-approval with Phase IV and real-world evidence (RWE) studies. Partner with us and leverage real-world data to demonstrate long-term safety and efficacy—keys to ensuring your continued success in a competitive landscape.

RWE & Post-Approval Studies