Search Results: Professional 156-587 Examinations Actual Questions - Easy and Guaranteed 156-587 Exam Success ☘ Easily obtain ⮆ 156-587 ⮄ for free download through ⇛ www.pdfvce.com ⇚ 💺156-587 Latest Exam Question
Study Activation: A Complex Process That Doesn’t Have to Be Painful
If the clinical development time of a new treatment is to ever decrease, reducing the time in study activation is necessary so actual research can be done.
Clinical Trial Efficiency: Top Risk Indicators and Solutions for Site Performance
Monitor four critical metrics across your sites to prevent persistent challenges to clinical trials
Screen Failure in Clinical Trials: Improving Reconciliation
Learn how screen failures occur and which three things to improve reconciliation can be done by those who manage clinical research.
Advarra Executive James Riddle Receives SRA International’s Best Concurrent Session Award
The Society of Research Administrators International (SRA International) has awarded James Riddle, Advarra VP of Institutional Services, its Best Concurrent Session Award.
Does This Study Require IBC Review?
While clinical research professionals are familiar with the role of the IRB to protect research subjects, most are unfamiliar with the added need for an Institutional Biosafety Committee (IBC).
Patient Engagement and the IRB
With increased efforts to engage and include patient and participant communities more closely in research, when does an IRB review become required?
Updated IRB Handbook Available
Advarra has updated its Institutional Review Board (IRB) Handbook for Investigators, Institutions, Sponsors, and Sponsors’ Representatives to version 5. Along...
Q&A Part II with Dr. Wendy Tate, Author of Insights Accrual Prediction Algorithm
This March, Insights Accrual Prediction platform was released to pilot customers. The second issue of our Q&A series continues our conversation with Dr. Wendy Tate, the author behind the machine learning tool’s algorithm, to hear her experience bringing this innovative tool to the research community and get her perspective on what comes next.
How to Improve Your Site Compliance
Many clinical trial sites face challenges to stay compliant on a study. It is important for sites to adhere to the myriad of requirements that constitute Good Clinical Practices (GCP).
Steps to Implementing a Quality Management System
Read our blog to learn more about quality, its role in clinical research, and how to implement a management plan.
A Tale of Two Sites: The Power of Integrated Research Administration
Learn how institutions attract more studies from the the tale of two sites: one with an integrated research administration, and one without.
Mobile Apps: Considerations for Use in Research Involving Human Subjects
Robert Neff and Michele Russell-Einhorn discuss considerations and issues research professionals should be aware of when developing research projects that involve mobile apps.
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