Jump back into the top resources from this month! ✅ See how DP Clinical, a high-achieving CRO with over 25 years of experience, improved study timelines and patient experiences with Medrio. ✅ Find out why a data strategy is important and how to build the right team to capture the attention of cautious investors. ✅ Learn how to build effective queries that reduce redundant checks, enhance data quality, and prevent costly delays. Read the September edition of our Resource Roundup 👇 #Biotech #Biopharma #CRO #EDC #eConsent #ePRO #eCOA
Medrio
Software Development
San Francisco, CA 9,856 followers
Powering your research potential.
About us
At Medrio, we're fueled by an ambitious vision: to improve 100 million lives by enabling secure, reliable, and efficient clinical trials. Since 2005, we have cultivated a thriving network of individuals who share a common goal of making a positive impact - including our dedicated team of Medrians, valued customers, and trusted partners. Our eClinical solutions are flexible and configurable to meet the needs of any clinical trial - from traditional to fully decentralized. Our solutions are easy to learn, easy to use, scalable and connected through one unified platform, providing unmatched efficiency, reliability, clarity and sophistication. As an employer, our core values are rooted in a customer-first approach, an A-player mindset, and a sprinkle of quirkiness to keep things fun and interesting. We are dedicated to powering the potential of clinical research - and we invite you to be a part of our mission. Visit our website to learn more, request a demo, or apply to join our team.
- Website
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http://www.medrio.com
External link for Medrio
- Industry
- Software Development
- Company size
- 51-200 employees
- Headquarters
- San Francisco, CA
- Type
- Privately Held
- Founded
- 2005
- Specialties
- Electronic Data Capture (EDC), eClinical, Electronic Case Report Forms (eCRF), Electronic Patient-Reported Outcomes (ePRO), Data Management, Clinical Research Organization (CRO), Phase 1-4, patient centricity, eCOA, eSource, Clinical Trials , Easy-to-use, RTSM, Randomization and Trial Supply Management, Electronic Consent (eConsent), Electronic Data Capture (EDC), and Clinical Data Management
Locations
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Primary
345 California Street
Suite 600
San Francisco, CA 94104, US
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1 St Katharine's Way
London, England E1W 1, GB
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2nd floor
Sai Apex 201, Viman Nagar,
Datta Mandir Chowk, Pune 411014, IN
Employees at Medrio
Updates
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🔵 Medrio demos live in San Francisco! 🔵 Clinical Data Management Innovations 2024 is just around the corner. If you’re on your way to the Bay Area, there’s still time to schedule a hands-on demo of Medrio. Our data strategy experts will walk you through everything from configurable, user-empowering database builds to real-time data access capabilities. See how the right clinical data management software can transform your study operations. Book your demo at CDMI today: https://bit.ly/3XipFrL #EDC #CDMS #eConsent #eCOA #ePRO #RTSM #ClinicalDataManagement #ClinicalTrials #DataQuality
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🚩 Is query management costing you time and money? Learn how to build effective queries that reduce redundant checks, enhance #DataQuality, and prevent costly delays in your #ClinicalTrials: https://bit.ly/46UTcuw
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🔵 Most CROs have extensive experience selecting technology solutions. Use their knowledge! Try requesting case studies and references from your CRO’s past partnerships to see how they implemented solutions for trials with similar requirements. Get the complete step-by-step guide for choosing an #EDC with your #CRO here: https://bit.ly/4docjzi
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📌"The programming is just so easy... Medrio’s drag-and-drop interface makes it simple." - Matthew Jachowski, Senior Technical Clinical Data Manager at DP Clinical Inc. See how Medrio streamlines clinical operations for DP Clinical with more efficient database builds, pre-built form libraries, and three-tiered production and validation environments. Read the full success story here: https://bit.ly/3AGUEog
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The most useful asset for securing funding in today’s risk-averse landscape? 👉 Robust clinical trial data. Build confidence with our essential guide to funding for biotech and biopharma: https://bit.ly/3Z0UiDl
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📣 Heading to Clinical Data Management Innovations 2024? Don’t miss your chance to see Medrio in action! Jay Lomakin, Rod McGlashing, and Charles G. will be providing live demos of Medrio’s CDMS/EDC, eConsent, eCOA/ePRO, and RTSM solutions. Tell us about your studies and the unique challenges you want to overcome. We’ll provide a personalized recommendation for how Medrio can help! Reserve your spot here and beat the rush on the conference floor: https://bit.ly/3XipFrL
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🔴 Roadblock or milestone? A decision from the #FDA to delay Lykos Therapeutics’ MDMA-assisted therapy for PTSD was a huge blow to psychedelic drug developers, but it’s also been deeply informative. The FDA’s Complete Response Letter (CRL) offers extensive feedback for Lykos and other players in the space about how they can address the potential for abuse, long-term efficacy, and functional unblinding to secure approval in the future. One thing is abundantly clear if we want to get these life-changing treatments in the hands of people who need them: the industry needs high-quality, submission-ready data that speak to these risk factors. Read more about the FDA’s decision and the future of psychedelic therapies from BioSpace here: https://bit.ly/3WZ4vxj
FDA’s Lykos Rejection Delays—But Doesn’t Stop—Psychedelic Therapies
biospace.com
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Tired of dealing with excessive queries that slow down your #ClinicalTrials? It’s a common problem—ineffective queries can lead to frustration and wasted time. But did you know that carefully designed queries can make your data collection process smoother and more accurate? Learn how to build better queries and leverage a robust CDMS/EDC system to run your trials efficiently: https://bit.ly/46UTcuw
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⭐ If you’re a high-achieving #CRO, you want an eClinical partner who can meet your standards and support your customers. When DP Clinical Inc. needed to manage complex data collection and informed consent for an upcoming observational study, they partnered with Medrio. Dive into our conversation with Matthew Jachowski and Jim Hamer at DP Clinical. You’ll see why this experienced CRO has chosen Medrio as their eClinical provider for over 22 studies! Read the success story here: https://bit.ly/3AGUEog #EDC #eConsent #ePRO #DataQuality #ClinicalTrials