临床解决方案
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.
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.
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.
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.
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.
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.
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."
PV Automation
Fortrea is an incredible team who has stepped up each time.
MedTech—done right
Bring your medical device or diagnostic product to market with confidence. Our dedicated MedTech 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.
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.