News
Lindus Health Introduces Bespoke “All-In-One CRO for Digital Therapeutics” Solution to Companies In the Space to Streamline Clinical Trials
We're introducing our All-In-One CRO solution for the digital therapeutics market.
Interview: Robert Langer backs Lindus Health’s "anti-CRO" strategy
Robert Langer and Lindus Health co-founder, Meri Beckwith, sat down for a Q&A session to discuss their new partnership and future direction of the company.
Robert S. Langer, Co-Founder of Moderna, Joins Lindus Health’s Advisory Board
We are thrilled to announce Robert S. Langer, co-founder of Moderna, has joined our advisory board.
Being Nimble and Tech-Forward in Clinical Trial Operations
In our latest fireside chat, we sat down with Dan Gusz, Chief of Staff at Signos, to discuss some of the common challenges sponsors see when collaborating with CROs along with the benefits of being cutting-edge in technology when approaching clinical trials.
Lindus Health and Thirty Madison complete enrollment of personalized dermatology care pilot study
We're excited to announce the completion of enrollment in Thirty Madison's personalized dermatology care pilot study that we're delivering.
Product Clinic #9: Bringing about the right kind of change with AI
Amiel Kollek, senior software engineer at Lindus Health, reflects on the use of AI in clinical trials and how it can be used to bring about the right kind of change.
Drug Discovery is Becoming More $$$ — Here's Why, And How We're Fixing IT
Drug discovery is becoming more expensive and producing less results than ever before (Eroom's Law) —why? One of the ballooning costs is clinical trials. Our co-founder Meri Beckwith sits down with Dr. Mustafa Sultan, creator of The Big Picture Medicine Podcast, to talk through how we're building the anti-CRO (Lindus Health!) to solve this problem.
Discussing the FDA’s latest draft guidances on 510k submissions with M. Jason Brooke, Managing Member at Brooke & Associates
M. Jason Brooke, Attorney and Managing Member at Brooke & Associates, was kind enough to stop by our virtual fireplace to discuss the FDA’s latest draft guidances on 510k submissions and share tips on how medical device companies could best navigate them.
.png)

%2520(1).jpeg)
.png)




