Regulatory and Scientific Medical Writing

Thanks to a full portfolio of medical writing services, our clients have access to start-to-finish support for every clinical research text, including expertly crafted reports in compliance with ICH human use guidelines, clinical trial protocols, regulatory documentation, and other submission documents all the way to abstract and manuscript completion. Our oncology medical writers consult with your team—as well as therapeutic experts, researchers and academics—to develop a sophisticated and in-depth understanding of your program. Writing services vary by your needs and can include:

Ask us how you can get your clinical plan started today.