Insights, guides, and updates on clinical trials, research technology, and regulatory compliance.
We cannot always anticipate changes that might crop-up mid-study, but we can set the standard for a good amendment workflow. Here's how...
It's always comforting to have a point of contact - a person who knows you and that you can connect with. In trials this is hugely important in retaining trust.
Everyone has a choice in their preference of communication (or non-communication) type. How can we align participant needs with the study design when it is tech-focussed?
The concept of SDV has changed dramatically with the evolution of technology. How does this marry with remote monitoring of data submissions?
Smartphones, tablets and smartwatches - there are a lot around. When is the right time to standardise all devices? or enact BYOD?
As with many things in life, it's important to put yourself in someone else's shoes. What do participants need from an effective ePRO tool?
Reducing the number of steps we take in clinical trials to store and communicate data is always a good thing. How can we best achieve this?
Working with many sites can be difficult to coordinate in any trial. Selecting ones that work well - both ways - can be tricky.
Protecting participants, their identity and their data in human trials. Be responsible and do the right thing.
