Human trials in the UK typically need to be greenlit by the National Health Service (NHS). Avoid delays and constant changes by checking off some of these key items

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?

Engagement drives compliance! How do you keep participants engaged in your human trials?

Participants should be supported during human trials - often this can be through financial incentive. Here's how to navigate this tricky ethical territory

Clinical Research Associates (CRAs) and Clinical Research Coordinators (CRCs) are essential to trial conduct - how do they make their mark?

Are you aware of clinical trial phases? The concept and purpose of phases has evolved significantly over the last century

Is anonymity always required? How do you retain participant data rights in trials?

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

Both blinded and un-blinded trials need fair group allocation. Here's how you can manage proper randomization in your trials

Finding the right cohort for your trial can be difficult, but honesty and transparency are a must - Participant Information Sheet (PIS) essentials

What is the future of clinical trials process and methodology? Can DCTs help pave the way to better trials?