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Aetion has entered into an agreement to be acquired by Datavant, a leading health data platform company. Learn more →
Aetion is an industry-leading RWE standard setter with deep regulatory relationships.
As a trusted partner to global regulatory agencies and health technology assessment (HTA) bodies, Aetion sets the standard in advancing the use of real-world evidence (RWE) through transparent, fit-for-purpose methodologies and best-in-class scientific approaches. Our experts collaborate with leading industry groups to shape RWE best practices, while our peer-reviewed research redefines what it means to generate regulatory-grade evidence.
Aetion offers generous benefits to its full-time employees, which currently can include:
The benefits offering may differ based on geographies where employees are based, when outside of the United States.
Aetion’s solutions and experts help drive RWE standard advancement through collaborations with key industry groups, including:
A structured framework for creating a fit-for-purpose study design that can generate valid and transparent RWE
A structured framework for determining which datasets are fit-for-purpose to answer a given research question
SPIFD2 harmonizes SPACE and SPIFD templates, calls for articulation of the hypothetical target trial and sources of bias that may arise, and incorporates STaRT-RWE reference.
Aetion’s partnership with FDA began in 2018 with the launch of the RCT DUPLICATE project, led by Brigham and Women’s Hospital (BWH) and Harvard Medical School (HMS). This project aimed to replicate the results of 30 published RCTs to see whether the use of RWE would lead to the same regulatory decisions, the final results of which were published in JAMA.
Connect with us to work with the team advancing critical decisions in healthcare.