![](https://www.arisglobal.jp/wp-content/uploads/2023/06/shutterstock_750225187-copy-1024x576.jpg)
The European Union (EU) Clinical Trials Regulation (CTR) harmonizes the processes for assessment and supervision of clinical trials…
Learn More![](https://www.arisglobal.jp/wp-content/uploads/2023/03/paper-to-etmf-document-worker-1024x576.png)
Considering switching from a paper trial master file to an electronic one? There’s no better time than now. According to…
Learn More![looking at slide under microscope](https://www.arisglobal.jp/wp-content/uploads/2022/07/Blog-etmf-1024x742.png)
Managing your Trial Master File (TMF) is a necessary, and often tedious task for most clinical stakeholders—but it doesn’t…
Learn More