Blog26 June 2025 How a 3-Person Team Got to Phase 3 — Without the Overhead Gameto proves you don’t need a large CRO or a floor of data managers to run complex global... Learn more
Blog26 June 2025 From Hype to Health: What Sword Health Got Right About Evidence Sword Health didn’t follow the typical digital health playbook. Instead of rushing to market, they invested early in... Learn more
Blog23 April 2025 Building a Safer, Smarter Future: A Tiered Approach to AI in Life Sciences Adopt AI in clinical research with confidence using a risk-based framework that ensures privacy, security, and regulatory alignment. Learn more
Blog3 April 2025 Why a Life Sciences Museum Matters—And What It Can Teach Us About the Future of Medicine What a Museum of Medicine can teach us about trials, trust, and how the public sees (or doesn’t... Learn more
Blog27 February 2025 Build vs. Buy vs. Partner in Life Sciences: Making the Right Call How do you decide between building, buying, or partnering? Learn key decision factors and red flags to avoid... Learn more
Blog26 February 2025 Do CROs Need to Reinvent Themselves in 2025? A Deep Dive with Greg Licholai and Derk Arts High R&D costs aren’t due to a lack of innovation but inefficiencies in trials. Here’s how we can... Learn more
Blog5 December 2024 Local Labs in the EDC: Streamlining Safety and Efficacy Insights Local labs are a vital part of clinical trials, offering fast, cost-effective insights into safety and efficacy. But... Learn more
Blog30 September 2024 Waiver of Consent vs Waiver of Written Consent One is very common, the other is rarely granted. Learn the key differences between waiver of consent &... Learn more
Blog26 September 2023 A Digital-First Mindset Shift on eConsent eConsent plays a pivotal role in optimizing modern clinical trials, but the nuance around its adoption for pharmaceutical... Learn more
Blog14 August 2023 Preparing Your eConsent Study for IRB Approval In this blog we cover how eConsent benefits trials and aligns with IRB ethical commitments, how to prepare... Learn more
Blog9 May 2023 Unlocking the power of Real-World Evidence in FDA submissions An avalanche of data from so many real-world sources is available today, with the promise of more data... Learn more
Blog21 November 2022 AKRN optimizes patient assessment collection with Castor ePRO Castor's ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own,... Learn more
Blog16 November 2022 How EDCs are Changing the Game in Clinical Research An electronic data capture (EDC) system is software used to collect, clean, transfer, process, and store data in... Learn more
Blog12 October 2022 AKRN creates the ideal case report form using Castor EDC Learn how AKRN and Company Y were able to complete their 100-person study in nine months to help... Learn more
Blog22 September 2022 AKRN handles mid-study changes in medical device clinical trials with Castor EDC AKRN Scientific Consulting, a medical device CRO, used Castor's flexible EDC solution to handle constant mid-study changes for... Learn more
Blog9 September 2022 5 steps for patient engagement and better outcomes in decentralized clinical trials For successful decentralized clinical trials, researchers must encourage patient engagement. Learn 5 steps that modern companies are taking... Learn more
Blog16 August 2022 Automated data capture with eSource to train an AI algorithm Castor’s eSource platform streamlined collecting, capturing & processing large amounts of clinical data to train AusculThing’s AI algorithm. Learn more
Blog5 July 2022 Electronic Case Report Forms (eCRFs) in Clinical Trials: Shifting to a Modern Research Paradigm Castor is shifting the research paradigm for eCRF in clinical trials, transitioning from old, inefficient processes to a... Learn more
