Insights, guides, and updates on clinical trials, research technology, and regulatory compliance.
Keeping documentation up to date, fully transparent and up to regulatory standards can be tricky. Here are some of the most essential trials documents you should be aware of
Human trials often come with expectations of making some sort of claim. While that's very important, data quality is fundamental
Sites, sponsors and end-users... making EDC platforms work for everyone? Here are the essentials...
Is anonymity always required? How do you retain participant data rights in trials?
Set Phases to Run!
You need to conduct research across many borders in diverse populations and adhere to international ethical standards and practices. Here's how...
The term "GDPR" can incite fear and worry in the minds of many researchers. Here's what GDPR means for your human participant research
Regulatory authorities outline in great detail how a trial should be properly conducted. With technology, eSource can make things much easier for you
The DCT approach is not for everyone, but if you're looking to make the switch, what are the key questions you should be asking yourself?
