RWR Regs Pro
The ultimate guide.
Access detailed roadmaps and expert insights using our simple and elegant interface that effortlessly guides you through what you need to do to run your real-world research study; seamlessly combined with real-time regulatory updates…and so much more.
Not ready to start your study, but would love to run simulations on sucess factors related to disease prevalence, approval times, submission complexity or acceptability of biosampling etc?
Want access to real world research insights and state-of-the-art tools created by people who understand your challenges and pain points?
Want someone to listen to your frustrations and create elegant tools to address them?
Then, RedBird-RWR is the tool for you!
RWR Regs Lite
The basics. Our free, lightweight solution for when all you need are quick answers to simple questions about running your real-world research study. Previously, I (Stuart McCully) gave you this information through CHCUK.
RWR News
It’s just the news.
There is nothing more frustrating than pop-ups, sign-ups, ads and offers when you just want to relax and read the news.
Which is why we’ve created a real- world research news site (HawkEye News). It’s just news. No pop-ups, no ads, no bull, and a little added sprinkle of our magic.
RWR Consulting
The comfort blanket.
Real world research is a complex world, especially the nationally diverse regulatory requirements.
The good news is you don’t need to worry. We’ve got your back. We’ve done the hard work of collating, reviewing and verifying what you do (and don’t!) need to do.
So, sit back and relax.
RWR Study Master File
A study master file for observational studies. If I have a study that isn’t a clinical trial…how do I make the study documents fit into the clinical trial master file?!! We felt (and lived) your pain and frustration. You now have a solution tailored to your needs…