Get the Facts: NDA-Enabling Studies
We’ve Got Your NDA Study Needs Covered
The development of an NDA submission plan can sometimes be unclear. Partnering with the right CRO early on can increase your chances of success and ensure you meet your milestones. With over 25 years of experience across the spectrum of therapeutic areas, Altasciences' specialists apply their knowledge in designing, conducting, analyzing, and reporting on trials for regulatory submissions.
Our complimentary fact sheet guides you through the different types and features of NDA-enabling clinical pharmacology studies, and how we can support you.
Want to learn more about the requirements for each study? Explore these insightful resources: