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Study Activation Survey Results: Medicare Coverage Analysis (MCA)
Advarra conducted a study activation survey in 2020. This blog outlines the information analyzed surrounding Medicare coverage analysis.
Leveraging Data to Lead and Manage the Research Mission
This blog discusses how to use clinical data at all levels to lead and drive the research enterprise and day-to-day operations
Accreditation and Compliance
Advarra operates in compliance with US federal regulations, various guidelines as applicable, & the ethical principles of human research.
Why Keep HIPAA Separate from the Informed Consent Form
HIPAA is important to the informed consent process, and oftentimes, a standalone document is the most beneficial approach.
How Technology and System Integration Can Improve Your Billing Compliance
The consequences of inaccurate billing can be severe, and ensuring workflows are being followed by all teams across an institution can be a difficult process.
Q&A – Racial Diversity in Clinical Trials: Building Trust in Participant Engagement
Our experts answered some of the most popular questions from "Racial Diversity in Clinical Trials: Building Trust in Participant Engagement."
The Importance of Hazard Communications in Clinical Trials Involving Genetic Engineering
A formal hazard communication or IBC SOP is critical to ensure clinical personnel understand the risks involved with genetically engineered investigational products.
Enhancing Research Conduct Using eConsent
The Belmont Report established informed consent parameters in 1976, but there are no federal regulations surrounding electronic consent.
Key Considerations for Regulatory Compliant Document Storage
It is imperative that your organization has a reliable eRegulatory system and associated policies for storage and upkeep of clinical trial documents to ensure 21 CFR Part 11 compliance. Read our Key Considerations for Regulatory Compliant Document Storage.
Understanding FDA’s 2024 Draft Guidance on DMCs
Find out about the FDA current views regarding DMCs and the 2024 draft guidance’s implications for clinical trial sponsors.
Planning for Complex Change at Your Organization
Navigate the ever-changing landscape of innovation and technology in clinical operations by discovering strategies to help your organization.
Advarra Connect
A secure transfer of IRB-related documents directly from the CIRBI platform to your electronic trial master file.
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