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news roundup
The collaboration provides Parexel access to HealthVerity’s data sets including claims, electronic medical records (EMR), lab data and social determinants of health, using HealthVerity’s privacy-preserving technologies, to provide customized RWD solutions for clinical trial needs.
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Trends and Insights for Your Oncology Trial:
Tuesday, November 12, 2019 at 10am EST
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Veeva SiteVault Free, a free eRegulatory cloud solution built specifically for clinical research sites, allows sites to manage regulatory documents and trial processes and features capabilities such as electronic signatures, remote monitoring, certified copy workflows, and reporting. SiteVault Free has a planned for availability in December 2019, and sites can sign up for SiteVault Free ahead if its release.
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Launching Medical Devices in the Japanese Market
- How to navigate regulatory and reimbursement approval
Thursday, October 31, 2019 at 11am EDT
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Elligo Health Research has received a grant from the FDA for a follow-on project to extend the value of common data harmonization in the generation of clinical evidence from real-world data (RWD) to support regulatory use.
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Will Decentralized Clinical Trials Compound Patient and Data Quality Risks?
Tuesday, October 29, 2019 at 1pm EDT | 12pm CDT| 10am PDT
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Articles
In this peer reviewed article, the authors explore the use of DIY collection of small home-blood sampling in pediatric trials. They also discuss results from a focus group regarding their preferences, perceptions, acceptability, and benefit trade-offs between treatments and the burdens of clinical trial participation.
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GrantPlan: Create Grant Budgets with Confidence and Accuracy
Thursday, October 10, 2019 at 11am EDT
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Biotech companies founded in China are poised to sell their medicines worldwide and have started conducting clinical trials in the U.S. and internationally.
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Begin with the End in Mind: The Strategic Benefit of Coordinating Site Budgeting, Contracting, & Payments
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How AI/ML and advanced techniques are enhancing clinical development
Lessons learned from use in study design, patient and site ID, safety, and risk-based monitoring
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Blog Posts
With legacy data platforms no longer enough for the needs of modern clinical trials, machine learning based analytics solutions provide instantaneous views of an organization’s data and can be leveraged across multiple portfolios by sponsors and across multiple sponsors by CROs.
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Successful Early Phase Drug Development of mAb Drugs
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David Freeman, General Manager, Information Ventures, for Quest Diagnostics, discusses how Quest can leverage its laboratory data to be an effective partner for pharma and biotech firms with its Clinical Insights and Trials Connect capabilities.
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