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Clinical Tech Leader
互联网出版
Cranberry Township，Pennsylvania 1,154 位关注者
A community dedicated to those who harness technology to enhance clinical trial design and execution.
关于我们
Clinical Tech Leader is the only community exclusively focused on harnessing technology to enhance clinical trial design and execution, ultimately leading to improved trial outcomes and a better patient experience. In a world where clinical trial professionals face relentless pressure to expedite timelines while adhering to rigorous regulatory standards, this community serves as a beacon of innovation and collaboration.
- 网站
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https://www.clinicaltechleader.com/
Clinical Tech Leader的外部链接
- 所属行业
- 互联网出版
- 规模
- 51-200 人
- 总部
- Cranberry Township，Pennsylvania
- 领域
- life sciences和clinical technology
动态
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Discover how maintaining strong data integrity can transform your clinical trials and strategies you can use to optimize trial builds and streamline data collection processes, ultimately leading to faster approvals: https://lnkd.in/dGC-BCri Source:?Anju Software
The Role Data Quality Plays In Getting Your Product To Market
clinicaltechleader.com
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The clinical trials market worldwide reached $80.7 billion in 2023 and is expected to grow at a rate of about 6.5 percent from 2024 to 2030, according to a report by?Grand View Research, Inc. As clinical trials at all phases accelerate, the need to avoid costly delays and speed time to market is urgent. Learn how automation can help: https://lnkd.in/d5vxdvhy By Laura Acosta, VP of Product Management, eClinical Division, Anju Software
Accelerating Your New Therapies Path To Market With Automation
clinicaltechleader.com
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This three-part series will explore the use of computerized system compliance in clinical research beginning with a primer on two things: the predicate rules (regulations), guidance documents, directives, and guidelines; and the scientific method. By Richie Siconolfi, Richard M. Siconolfi, LLC https://lnkd.in/eaNeKhQN
How Technology Has Changed Computer System Validation
clinicaltechleader.com
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Even with R&D spending up from 44% over the decade to 2022, the number of U.S. novel drug approvals has stayed flat. In the face of this challenge, clinical trial managers seek ways to improve efficiency and streamline clinical trial operations. Discover how integrated digital solutions can help address significant operational challenges that raise costs and prolong trial durations. https://lnkd.in/eFR8A9sR By Laura Acosta, VP of Product Management, eClinical Division, Anju Software
Avoid Clinical Trial Operation Delays With Streamlined Digital Solutions
clinicaltechleader.com
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In this on-demand discussion, a distinguished panel of experts illuminate the crucial role of patient-reported outcomes (PROs) in shaping regulatory decisions and drug development strategies, particularly in light of FDA expectations. https://lnkd.in/eT7Gsp5K Source:?Castor
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Learn how to combat the instrument licensing and linguistic validation challenges associated with adopting electronic Clinical Outcome Assessments (eCOA), ensuring quick access to source files: https://lnkd.in/evMTeu-E By Willie Muehlhausen ???? and Tim Davis, Veeva Systems
Addressing The Challenges Of eCOA Licensing
clinicaltechleader.com
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"The Validation Specialist" Richie Siconolfi explores computerized system compliance in clinical research in this three-part series, beginning with a primer on two things: the predicate rules (regulations), guidance documents, directives, and guidelines; and the scientific method. https://lnkd.in/emCAQ8MF
How Technology Has Changed Computer System Validation
clinicaltechleader.com
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Learn how proactive planning by sponsors and early User Acceptance Testing (UAT) involvement in the eCOA design process can substantially improve study quality, efficiency, and consistency. https://lnkd.in/eqjEFjQB By Gauri Nagrani and Tim Davis, Veeva Systems
Shaping The Future Of eCOA User Acceptance Testing
clinicaltechleader.com
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In this on-demand webinar, delve into pragmatic approaches for clinical evidence generation and regulatory acceptance. This discussion examines recent FDA draft guidance on integrating RWD/RWE in medical device studies and explores case studies of companies effectively leveraging RWE. https://lnkd.in/eu5c3T5P Presenters: Craig Serra, Flatiron Health Josh Buddle, Flatiron Health Jonathan Helfgott, The Johns Hopkins University Tara Marti, Exact Sciences
Applying RWD: Use Cases And FDA Guidance
clinicaltechleader.com