Tips for meeting the ClinicalTrials.gov requirements
We share a few tips to help you ensure
Menu
Providing opportunities to learn tips & tricks from our in-house subject-matter experts and discover more about Bright culture.
We share a few tips to help you ensure
Our favorite clinical sites share these four characteristics.
As a working mother, our CEO understood the challenges
Part 2 in our series: Prepare, Launch/Maintain, & Close
Our Chief Scientific Strategist talks all things statistics and
Part 1 in our series: Define, Refine, and Freeze.
5 tips for a successful publication journey.
The trickle-down effects of change are often underestimated.
Swift IDE approval is possible when your submission convinces
Welcome back to part two of our blog series
The saying “The only constant in life is change”
A primer on controlling statistical error.
Are you pulling your hair out trying to engage
BRIGHT study leads are the best at what they
A well-planned site selection process is essential for the
When bias creeps into a clinical study, the result
When you partner with experienced and capable investigators and
In celebration of Earth Day and the sense of
The randomized controlled trial (RCT) is the gold standard
What did the case report forms say to the research coordinator? You
Most leadership teams would agree that it is better
When a clinical study will be used to support
It may seem counterintuitive that collecting too much data
Every medical device clinical study has endpoints, although they
As I prepare to retire from my long and rewarding career
Avoid costly surprises during the study or regulatory application
Work-life balance. Mindfulness. Self-care. Is there a fly in
You are developing a medical device that addresses a
The pre-sub meeting process can be a powerful tool.
The medical device product development cycle can take several
