2025 Year in Review
As we close out 2025, we’re feeling proud of…
Providing opportunities to learn tips & tricks from our in-house subject-matter experts and discover more about Bright culture.
Informed consent form practices could be improved by applying…
2024 was a productive and successful year for Bright…
Clinical studies are all about the people – the…
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…
Bright’s 6-step clinical study development process.
5 tips for a successful publication journey.
During the past few months, I’ve raved to family…
The trickle-down effects of change are often underestimated.
Swift IDE approval is possible when your submission convinces…
Sustainability is both a priority and a passion at…
Welcome back to part two of our blog series…
The saying “The only constant in life is change”…
Gain background—and confidence—for creating statistically sound studies.
Are you pulling your hair out trying to engage…
Learn the business side of managing clinical studies.
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…
Bright’s 6-step clinical study development process.
When a clinical study will be used to support…
Discover the pitfalls of—and tips for avoiding—this common problem.
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.
