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| Webinar: Unleash the Power of IQVIA Complete Consent | The eConsent market is evolving, focusing on improving patient experiences, streamlining clinical trial processes, and global expansion. Staying informed on industry developments is crucial. Discover the market's trajectory, explore IQVIA Complete Consent's cost-effective tailored solutions for all sponsors and study types, and get an exclusive look at the Interactive and Simple PDF modules highlighting new features, capabilities, and much more! Click here to learn more. |
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CLINICAL TRIAL TECHNOLOGY |
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| Document Processing: A New Hope | Webinar | Cencora PharmaLex | Tired of slow, error-prone document processing? Discover how top companies are boosting speed and accuracy while slashing costly rework. Watch now to learn how you can achieve TMF excellence faster. |
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| IRT? RTSM? What's The Difference? | Article | Perceptive Inc | What are the components of Randomization and Trial Supply Management (RTSM) and the critical role of RTSM and Interactive Response Technology (IRT) in clinical trials? |
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| The Workhorse Of Today's Clinical Trials | Article | OpenClinica | Unlock the power of decentralized clinical trials with an electronic data capture platform (EDC). Discover how stakeholders benefit and what to consider when choosing the right EDC system. |
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| With ICH M11 expected to be adopted by the end of the year, the next Clinical Leader Live digital event will host a panel discussion on the advantages of improving and simplifying the dataflow of clinical trials but also the challenges associated with creating a connected digital dataflow, including digital health channels, that spans from protocol to data collection to CSR. Register today and join us on 10/31 at 1 pm ET (10 am PT). |
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| DIA Canada Annual Meeting | November 14-15, 2024 | Gatineau, QC, Canada The DIA Canada Annual Meeting will provide an in-depth exploration of the current pharmaceutical, medical device, and diagnostic landscapes in Canada, emphasizing Canada’s pivotal role in global healthcare product development. Offering three specialized tracks on Regulatory, Clinical, and Safety and Pharmacovigilance, the meeting will cover topics spanning from Health Canada’s latest regulatory initiatives, international collaboration, and innovative clinical practices to approaches that harness AI in drug safety and increase representation from equity-denied groups. Attendees will have the opportunity to engage with leaders and experts from academia, regulatory bodies, and the pharmaceutical and medical device industries by gaining insights into best practices, lessons learned, and strategies to address the challenges facing stakeholders in Canada. Learn More. |
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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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