Your drug has passed through the phase I clinical trial and you’ve selected and contacted the sites you want to work with. Now it’s time to get your trial up and running in the EU. What do you do? Let’s walk through the process step by step. At Siron Clinical, we...
At first glance, it’s abbreviation soup – EMA, FDA, NIHR, OHRP, IRB – but this collection of organizations is responsible for making sure clinical trials are run properly, to protect patients and develop medicines that are safe and effective. However complex it seems,...
A clinical trial involves complex overlapping processes, many of which require specialized expertise and experience. So how can you run a clinical trial successfully if you don’t have the expertise in-house? That’s where a CRO comes in. What Is a CRO? A contract...
As a CRO, we talk about clinical research and clinical trials, but what’s the difference? Can the two terms be used interchangeably? And why does it matter? Every treatment on the market is the result of years of research – not just studies involving the treatment...
How does the Siron Clinical team ensure the success of our clients’ clinical trials around the world? Let’s take a look behind the scenes at people’s roles and how they work together. When Jan Balemans, Founder and CEO of Siron Clinical, started the company in 2000,...
