Accelerating Study Start-up Regulatory Submission in Sub-Saharan Africa
Conducting clinical trials in Africa has many benefits. But sometimes the regulatory approval can be a drag.
Learn how ACE Research uses proprietary regulatory intelligence database, country-specific guidelines, and project-specific regulatory tracker to streamline
the collection of site essential documents,
QA regulatory package
submission of the final dossier to the ethics committees and national regulators,
We ACE regulatory submissions to the ethic committee and the regulatory authorities, making the process
aligned to the format and style of Africa regulators