For over 30 years, PAREXEL has proven to be a trusted partner for the complex development journey required of biopharmaceutical and medical device companies. We’re also an astute guide, able to simplify that journey for our clients, so safe new products can reach patients more quickly.
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What do we do?
Globally Integrated Science Taking Your Journey to Global Markets
It can be a long and complex journey, taking your scientific innovations out to the world. This is only the first reason why PAREXEL® is the perfect partner to help you get there. As one of the world’s largest and most experienced biopharmaceutical service providers, we have the global infrastructure, harmonized protocols, and advanced technologies to uncomplicate the process for you, accelerate your time to market and contain your development costs while minimizing risks of late phase failure. It all begins with our end-to-end approach to conducting clinical trials.
From feasibility analysis, site selection and patient recruitment to clinical monitoring, data collection and management on through NDA preparation, submission, and post-approval studies, PAREXEL is committed to your entire journey.
Whatever the size or scope of your study, PAREXEL provides the comprehensive clinical research services you need, from First-in-Human through Phase IV and Post-marketing follow-through. We also have the regulatory expertise, clinical trial operations management, payer and market access planning, medical education and communications capabilities to see your journey through efficiently and effectively.
Explore every phase of our clinical services for a complete picture.
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