??Winning funding in a risk-averse market isn't just about having cutting-edge technology. A product’s commercial potential and the team behind it are the factors that often make or break a deal. Learn what biotech investors are looking for in the teams they fund. Read our report with BioPharma Dive: https://bit.ly/4952fdn
关于我们
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.
- 网站
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https://www.medrio.com
Medrio的外部链接
- 所属行业
- 软件开发
- 规模
- 51-200 人
- 总部
- San Francisco，CA
- 类型
- 私人持股
- 创立
- 2005
- 领域
- 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)和Clinical Data Management
地点
Medrio员工
动态
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?? #AI has the potential unlock new discoveries at a previously unimagined pace, but the stakes are high. Poor application of AI can put patient safety and data integrity at risk. It’s crucial to understand how regulators recommend approaching AI when considering it for your clinical trials. Our blog breaks down the latest regulatory guidelines from the US, EU, UK, Canada, and China. From stringent data accuracy standards to guidelines for AI-enabled devices, there’s a lot for clinical researchers to stay on top of. Help keep your AI-enabled trials compliant, safe, and innovative. Read the blog here: https://bit.ly/4eGotnn #ArtificialIntelligence #ClinicalTrials #CDMS #EDC
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?? Join Team Medrio as our Director of Product Management! We’re seeking an experienced, visionary leader with a deep understanding of the eClinical landscape to lead our EDC and eCOA product strategy. In this role, you'll: ? Develop and execute a comprehensive product roadmap ? Define product positioning and develop go-to-market strategies ? Lead cross-functional teams to ensure successful product launches ? Be the voice of the customer, ensuring our solutions meet their needs If you have product management experience in the life sciences or healthcare technology sectors—and you're excited to steer the future of eClinical technology—we’d love to talk to you! Learn more about the Director of Product Management role and apply here: https://bit.ly/3YMIJhe
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??Unlock the secrets to early-phase success–join our webinar on Dec. 3rd! Clinical trial experts Nicole DuPont Latimer, Kate Porta Smith and Bryan Terry are teaming up to bring you actionable insights on: ??Designing scalable trials that support future growth ??Ensuring data integrity to meet regulatory milestones ??Selecting the right CDMS/EDC to handle evolving trial demands Navigating complex regulatory landscapes and handling increasing volumes of data as you progress through early-phase trials is no small feat. But with the right data and technology strategy from the start, you can pave the way for long-term growth. Register for the webinar here: https://bit.ly/3O9X4zm #ClinicalTrials #EarlyPhase #EDC #CDMS #DataQuality #DataManagement
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???? Database lock in just 13 days? Yes, it’s possible! This playbook reveals Medrio’s proven strategies for closing the gap between Last Patient Last Visit (LPLV) and database lock to keep your clinical trial timelines on track. Get access to best practices, FAQs, and a glossary of terms from Medrio’s data science experts Muhammad Bilal and Rod McGlashing. Understand how to streamline database lock and your path to study closeout. Download the eBook here: https://bit.ly/4hOjxiT #ClinicalTrials #DatabaseLock #EDC #CDMS #DataQuality
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?? ?? Helping the people who help people. At Medrio, that's our every day. We asked Rochelle Shearlds, Nicole DuPont Latimer, and Chris Dixon what inspires them about working at Medrio. Watch to see why these Medrians value the collaborative journey with our customers to bring clinical trials to those who need them most ??
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?? Multi-site challenges for Clinical Trials Resource Group, LLC – solved! ?? Dive into our latest case study with this experienced CRO. See why clinical operations experts value Medrio’s study build support, user-friendly features, and proactive data management approach: https://bit.ly/48Y6Iil
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?? The road to submission for medical devices can be rocky. You’re contending with new study complexities, rigors in data collection, and tighter funding. But you don’t have to navigate these roadblocks alone. In our latest eBook, MedTech-minded solutions experts Rod McGlashing and Tina Caruana are here to help you plan for successful regulatory submission. Find out what you should know as you plan your clinical trial roadmap, including: ?? Regulatory trends impacting medical device trials ?? Best practices for protocol development and data management ?? Must-have tools to streamline your trial process Ready to give your device the best shot at approval? Download the eBook here: https://bit.ly/40xXRRZ #ClinicalTrials #MedicalDevices #EDC #CDMS #ePRO #eConsent
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?? It happens in almost every study—data is misplaced, out of range, or unreadable. Queries are essential to validate this uncertain data, but excessive or poorly built queries can increase costs. Want to build queries that ensure high-quality data and efficient processes? Read our blog: https://bit.ly/3UDZvOb #ClinicalTrials #EDC #CDMS #DataQuality #DataManagement
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? AI is a powerful tool for data collection and management, but it’s human expertise that turns AI’s insights into actionable steps. In this snackable infographic, learn what implications AI can have on data quality, trial costs, and study timelines and how you can ask the right questions to stay on track. ?? Download the infographic here: https://bit.ly/3UxDj8G #ArtificialIntelligence #AI #ClinicalTrials #DataManagement #DataQuality
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