Insights, guides, and updates on clinical trials, research technology, and regulatory compliance.
If you're conducting human participant research in the UK, you will need to be aware of IRAS
There are many ePRO systems available with many offerings, but what are the most useful features that will help you?
Standard Operating Procedures (SOPs) ensure proper trial conduct to regulatory guidelines and frameworks - how should you work yours according to best practices?
An in-depth look at the top 10 most communicated points surrounding data collection in human research
Protecting your data should be a top priority - whether it's sensitive intellectual property or private health records
Data collection comes with many challenges - whether you're using traditional methods, hybrid or all-in-one software approaches. Here are the most communicated issues from researchers worldwide
Addressing one of the most fundamental questions in data collection. Is my work even 'research'?
What are the obstacles to success in your trials? 8 things you need to be aware of
The two main types of trials - Intervention and Observational. Here are the differences and what they mean for you