Research Site Perspectives on Sponsor-provided Technology
Gain insights into site challenges with sponsor-provided technology, including system preferences, time metrics, and investigator platform experiences.
Expedite Study Startup: Four Strategies to Optimize Site Activation
Learn how organizations can expedite study startup and avoid delays through streamlining site selection, training, ethics review, and site initiation.
Canadian Medical Device Regulation 101
Download a larger version of the infographic Canadian Medical Device Regulations 101 Speed the research ethics board (REB) review process
Top-Tier University Stays Compliant with Advarra’s HRPP Assessment
A leading healthcare system partnered with Advarra for a Clinical Research Operations Assessment, enhancing compliance, mitigating risks, and strengthening their HRPP.
The Rise of the Clinical Research Network: Using Technology to Connect Sites and Sponsors
Explore how integrated technology solutions can reduce inefficiencies, improve diversity, and streamline workflows in clinical research.
Video: Custom eLearning Case Study at NCI-Designated Hospital System
As the pandemic continues, finding efficient ways to train employees in a repeatable and scalable way is crucial. Lauren Talley,
Planned Emergency Research and Exception from Informed Consent
Explore the regulatory criteria and ethical considerations for planned emergency research, including exceptions from informed consent (EFIC).
What Level of IRB Review Does Your Study Need?
Many research professionals do not realize that there are several different types of institutional review board (IRB) review. A study’s
Advarra Trend Report: The Future of Clinical Staff Development Planning
The report provides information based on surveys and interviews with organizational leaders from top U.S. biotech and pharmaceutical companies.
Ensuring Success with Clinical Development Planning
This white paper outlines key elements of a CDP, including Treatment population, Demonstration of efficacy, Demonstration of safety, Clinical supplies, and Timing of activities.
The Clinical Development Plan: Executing the Clinical Strategy
This white paper outlines key elements of a CDP, including Treatment population, Demonstration of efficacy, Demonstration of safety, Clinical supplies, and Timing of activities.
Reporting to the IRB: What Does and Does Not Need to be Reported
Learn the essentials of IRB reporting, including why it matters, what’s required, what’s not, and tips to avoid common reporting challenges.