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From Simulation to Success: Stress Testing Your Inspection Readiness
Gain expert insights, best practices, and strategies to navigate FDA inspections with confidence.
Executing a Successful Clinical Strategy
A clinical development plan is designed to bring an investigational medicinal product to market through outlining risks and opportunities to a program.
Advarra Publishes the State of Clinical Trial Activation at Sites Report
The report outlines actions to streamline study activation and maximize operational efficiency, making clinical research safer, smarter, and faster. (COLUMBIA,...
The Impact of Public Perception of Clinical Research
News stories in the past year were dominated by COVID-19 vaccine development. Everyone’s interested in the story, but how many know the ins and outs of vaccine development and how that affects research?
Keys to Advancing Your Biotech Go-to-Market Plan
Essential keys for growing biotech companies on navigating the complexities of the FDA 510K filing process.
Custom eLearning
Help your team customize existing content to align with your organization’s workflows, policies, and configurations.
ABSA International Appoints Advarra Executive Daniel Eisenman as Scientific Program Committee Co-Chair
The American Biological Safety Association (ABSA) International appointed Daniel Eisenman, PhD, RBP, SM(NRCM), CBSP, Advarra Executive Director of Biosafety Services,...
Expanding Our Global Consulting Expertise to Solve Mission-Critical Issues
Elevating our consulting capabilities to accelerate clinical research and bring therapies to market sooner.
GxP Services
Industry-leading GxP quality solutions designed for the rapidly changing life sciences and consumer products markets.
Privacy Regulations Impact on Global Clinical Trial Endpoint Adjudication
Endpoint adjudication committees must keep up with rapidly developing requirements as they receive potentially identifiable research data.
Certificates of confidentiality and unexpected complications for pragmatic clinical trials
Judith Carrithers co-authored the article "Certificates of confidentiality and unexpected complications for pragmatic clinical trials" in Learning Health Systems.
Improving Study Activation Time for Gene Therapy Research
With the growing popularity of gene therapy research and genetically engineered vaccines, sites need to understand study activation impacts
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