Introducing our latest CRO offering for the development of cardiovascular interventions.
December 10, 2024
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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.
January 30, 2024
Lindus Health Releases "All-in-One Cardiovascular CRO" Offering for Clinical Trials Serving Cardiovascular Health
Robert S. Langer, Co-Founder of Moderna, Joins Lindus Health’s Advisory Board
1/25/24
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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
1/24/24
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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
12/14/23
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
12/4/23
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
11/1/23
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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
10/25/23
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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.