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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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CLINICAL DATA MANAGEMENT & ANALYSIS |
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| A New Pharmacovigilance Ecosystem: Automation And AI | Guest Article/Blog | By Humaira Qureshi, Qinecsa, DIA | As Pharmacovigilance (PV) evolves into a proactive, value-driven discipline innovations like robotic process automation and artificial intelligence help improve efficiency and data utility. |
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| Are You Using Real-World Evidence? | e-book | Parexel International | This series of case studies illustrates how Real-World Evidence (RWE) can enhance decision-making processes and lead to more efficient development strategies that save both time and costs. |
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| Leveraging An Insight-Driven Trial Strategy | Article | IQVIA Research & Development Solutions | Discover how strategies guided by insights will influence the ever-changing clinical trial scene, underscoring the significance of actively engaging patients to enhance the design and execution of trials. |
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| Diving Into Data From Population To Subject | Brochure | Revvity Signals Software, Inc. | Explore Revvity’s Clinical Data Review Discovery solution, designed to instantly drill down from the population level to the subject level and present a more comprehensive view of the data. |
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| Simplify The Complexities Of RWE Generation | Brochure | Castor | By accelerating your research processes, see how this will also help in achieving more reliable outcomes, ultimately supporting the development of effective treatments and therapies. |
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| The DCT Revolution Is Over… Vive La DCT Evolution! | Article/Paper | By Life Science Connect Editorial Staff | The DCT ecosystem has matured significantly to include service providers with more real-world experience and advanced tools, plus a mindset of initiative versus reaction. Numerous regulators have released or updated DCT guidance documents in recent years, too, putting the onus on the industry to provide actionable feedback on those drafts. |
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| The Critical Role Of The Medical Monitor | Article | By Katie Dawson, inSeption Group | Medical Monitors interact with nearly all functional roles on a study team and more experienced monitors often support and mentor less-experienced colleagues. |
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| Optimize Protocols For More Successful Trials | Video | Citeline | Find out how you can harness the power of AI and world-class data to recommend endpoints and inclusion/exclusion criteria for streamlined protocol design that results in more positive trial outcomes. |
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| Clinical Medical Monitoring | Brochure | ThoughtSphere | Check out this all-encompassing module that simplifies and automates the medical review process, allowing medical monitors to prioritize the most crucial aspect – patient safety. |
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CHOOSE YOUR OWN ADVENTURE |
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| You're receiving the Friday edition of the Clinical Leader newsletter, focusing on Clinical Data Management & Analytics and Trial Monitoring. 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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