?? Calling all research sites and institutions! Registration for Onsemble, the premier conference for the research community hosted by Advarra, is live! With 40+ sessions presented by industry thought leaders to networking opportunities with leading research institutions, the customer-exclusive event presents a unique opportunity for research professionals to: ? Explore best-in-class, innovative technology solutions and services ? Engage in valuable discussions and interactive sessions led by industry experts ? Learn best practices from leading research institutions ? Enjoy networking events and make meaningful connections with peers ? Collaborate to find solutions for the industry’s most pressing challenges Hear more from Advarra SVP, Site-Sponsor Innovation Christine Senn, PhD, then learn more and register here: https://lnkd.in/gjzZ7c8F
Advarra
制药业
Columbia,Maryland 58,458 位关注者
Advancing clinical research: safer, smarter, faster
关于我们
Advarra advances the way clinical research is conducted: bringing life sciences companies, CROs, research sites, investigators, and academia together at the intersection of safety, technology, and collaboration. With trusted IRB and IBC review solutions, innovative technologies, experienced consultants, and deep-seated connections across the industry, Advarra provides integrated solutions that safeguard trial participants, empower clinical sites, ensure compliance, and optimize research performance. Advarra is advancing clinical trials to make them safer, smarter, and faster. For more information, visit advarra.com.
- 网站
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https://www.advarra.com/
Advarra的外部链接
- 所属行业
- 制药业
- 规模
- 501-1,000 人
- 总部
- Columbia,Maryland
- 类型
- 私人持股
- 创立
- 1983
- 领域
- Central IRB、Human Subject Protection、IRB Services、Clinical Research、Independent IRB、Institutional Review Board、Ethics Review、IBC Services、GCP Consulting、Compliance Consulting、Clinical Site Audits、CQA (Clinical Quality Assurance)、GXP Consulting、Human Research Protections、GLP Consulting、GMP Consulting 、Clinical Trial Management System、eRegulatory Management System和Clinical Data Management
地点
Advarra员工
动态
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The idea that many principal investigators (PIs) only participate in one clinical trial before leaving has been debated for years. But what does the data actually show? And should the industry be worried? Join Advarra's Elisa Cascade alongside fellow experts from SCRS, Tufts Center for the Study of Drug Development, Clinical Trials Transformation Initiative (CTTI), Continuum Clinical, A Spectrum Science Company, and Clinical Leader, as they break down the research, share insights, and discuss potential solutions in this upcoming webinar. Don’t miss this data-driven conversation on a critical issue in clinical research. Register here: https://lnkd.in/g9q3PBvH
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The site feasibility process is often seen as cumbersome, inefficient, and frustrating—but could CROs be the key to improving it? In a recent Contract Pharma article, Advarra's SVP of Site-Sponsor Innovation Christine Senn, PhD explores how the industry can rethink site feasibility and the role CROs might play in making the process more effective. Check it out here: https://lnkd.in/guGVT5yt #FasterTogether
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AI is transforming clinical research—from generating synthetic brain image data to influencing real-world evidence. With the EU AI Act introducing new regulations and the FDA finalizing guidance, what does this mean for HRPPs, IRBs, and research ethics? Join James Riddle's session today at the NWABR IRB Conference as he unpacks: ???Emerging AI use cases in research ???How new regulations will impact HRPPs ???Practical steps to prepare for an AI-driven future Be part of the conversation shaping the future of AI in research oversight. Learn more about the 2025 IRB, IBC & IACUC Conference series here: https://lnkd.in/gFXirGV9
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Thank you to our panelists Jamie Bendrick-Peart from AstraZeneca and Christina Brennan, MD from Northwell Health, as well as our moderator Christine Senn, PhD, for the impactful insights and discussion during our recent webinar, "Current State of Site-Sponsor-CRO Collaboration." Your discussions on communication challenges and strategies for improving efficiency in clinical trials were invaluable. For those who missed it, we reviewed the 2024 State of Site-Sponsor-CRO Collaboration Survey Report and explored steps to streamline processes in clinical research. Watch the full webinar on-demand here: https://lnkd.in/gxK5QWkP
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We asked the Advarra team to share why they choose to dedicate their careers to clinical research. Thank you for sharing, Leah Woughter! We'd love to know what drives your passion for clinical research in the comments below.
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Clinical research sites are under immense pressure—rising protocol complexity, staffing shortages, and financial strain are pushing many to the brink. What can be done to ensure their survival? In a recent interview with BioSpace, Advarra’s Chief Product Officer, Elisa Cascade, shares her insights on the challenges sites face and how collaboration, technology, and financial support can make a difference. Check it out here: https://lnkd.in/g5KxZxh7 #FasterTogether
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Join us at Onsemble 2025, where OnCore users from leading research sites will share real world insights, best practices, and strategies for optimizing clinical trial operations. This year’s lineup includes leaders from Yale University, Northwell Health, Arkansas Children's Research Institute, and University of California, Davis. If you’re an OnCore user, this is your opportunity to learn from peers, gain actionable takeaways, and enhance how your institution manages trials. Don’t miss these featured sessions designed for OnCore users! Secure your spot at Onsemble 2025 today here: https://lnkd.in/gjzZ7c8F Thank you to Joe Stokes, Brian Sevier, Eric Borchardt, Karen Luna, Amanda Childs, Kari Allen, Christina Brennan, MD, James Riddle, Kimberly Voight, Rachel Stevens, and Joe Matthews. Looking forward to hearing your sessions this spring!
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Join us for this Xtalks webinar on March 13 featuring expert speakers from Advarra, Parexel, and Takeda. These industry leaders will?dive deep into critical milestones in study startup such as site selected, contract finalized, greenlight packet approved,?and ready to enroll.?They'll explore how the right combination of people, process,?and technology can improve the way sites and sponsors collaborate during study startup, ultimately enhancing visibility and alignment across stakeholders?while avoiding common hurdles and headaches. Thank you to Ashley Davidson, Karen McIntyre MSc Clinical Trials, and Andrew Taylor for participating! ?? Register for this webinar now to explore how study startup milestones can be streamlined: https://lnkd.in/ex55cGA8
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