RESOURCE CENTER

An abstract photo of someone creating a timeline, with text displayed saying "Building Your Early Phase Clinical Data, From Protocol to Regulatory Submission"

Scientific Journal

Building Your Early Phase Clinical Data, from Protocol to Regulatory Submission

The Altascientist | Issue 29

Quality, reliable data is the key to successful drug development. In this issue of The Altascientist, take a deep dive into the complex, multi-step data journey for Phase I clinical trials, from conceptualization and initial protocol development, collection and analysis, through final regulatory submission.

Start Reading

RESOURCE CENTER

Building Your Early Phase Clinical Data, from Protocol to Regulatory Submission

SELECT A CATEGORY BELOW

Sign up for exclusive content

Stay connected