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| Webinar: Bridging the Gap: EHR to EDC Integration in Clinical Trials - Reality Check | The promise of seamlessly mapping data from Electronic Health Record (EHR) systems to Electronic Data Capture (EDC) systems has captured the attention of clinical research professionals worldwide. Join our distinguished panel of experts representing the critical perspectives of research sites, pharmaceutical sponsors, and Contract Research Organizations (CROs) for an engaging, honest discussion on the state and future potential of EHR-to-EDC integration. |
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CLINICAL TRIAL TECHNOLOGY |
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| Ask An Expert Before Shredding Your Mobile Device CAPEX | Guest Column | By Brad Grimes, mobile device provisioning and logistics consultant | Tasked with buying your company's mobile devices and not sure where to start? Discover the questions you should ask and the information you need to know before consulting an expert. |
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| Future Predictions For Clinical Technologies | Article | By Kees Van Ooik, Almac Clinical Technologies | In 2025, sponsors are prioritizing configurable, interoperable solutions that integrate seamlessly across IRT, eCOA, CTMS, eConsent, and supply chain systems. |
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| The Top 5 Myths About eCOAs In 2025 | Webinar | Medable | Join leading clinical experts as they debunk the top 5 myths about eCOA in 2025, separating fact from fiction to help clinical operations, procurement, and data management teams make smarter decisions. |
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| Level Up Your Supply Chain Initiatives | Article | IQVIA Technologies | Shipping and storing advanced therapeutics are complex processes, but advancements in accountability, wearables, and technology capture real-time factors critical to safety and protocol. |
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| NetSuite For The Biotechnology Industry | Product | Sikich | Biotech companies progressing through clinical trials, have a unique set of financial, contract, compliance, and reporting needs. This ERP solution is designed to address all of those needs. |
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| Overview Of Central eSource From CRIO | Video | CRIO | Central eSource transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework. |
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| The Rare Trials Summit brings together biopharma leaders, researchers, patient advocates, and regulators to accelerate the development of rare disease therapies. Over two days in Boston, attendees will engage in high-impact sessions, interactive workshops, and networking designed to spark collaboration, solve operational challenges, and improve patient outcomes—turning innovative ideas into actionable strategies for rare disease clinical trials. |
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CHOOSE YOUR OWN ADVENTURE |
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| You're receiving the Tuesday edition of the Clinical Leader newsletter, focusing on Clinical Trial Technology. To make changes to your newsletter selections, update your topic preferences. - Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
- Clinical Trial Technology (Tuesday)
- Decentralized Trials | Trial Management (Wednesday)
- Outsourcing Models | Regulatory & Compliance (Thursday)
- Clinical Data Management & Analytics | Trial Monitoring (Friday)
Learn more about our personalized newsletters here. |
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