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Advarra Trend Report: The Future of Work in Clinical Research
Download our report to learn more how the COVID-19 pandemic impacted the future of the clinical research workforce.
Clinical Trial Superheroes
Download this eBook to learn about the individuals who dedicate their talents to give patients an opportunity for healthier and longer lives.
PharmaVOICE Features Advarra CEO in “New Era of Clinical Trials” Cover Story
PharmaVOICE recently featured Gadi Saarony, CEO at Advarra, in its cover article “A New Era of Clinical Trials” discussing how the research industry’s response to the COVID-19 pandemic “will set the course for drug development for years to come.”
Expedite Study Startup: Four Strategies to Optimize Site Activation
Learn how organizations can expedite study startup by streamlining site selection, training, ethics review, and site initiation.
Inside Study Activation: Budgeting Takeaways
Learn how sites, sponsors, and CROs can work together to help study activation, specifically within budgeting and contracting.
Advarra Expands Review Capabilities for Cosmetics Research
Early Phase Center of Excellence now includes enhanced processes and increased expertise for research involving cosmetic products (Columbia, MD.) Advarra,...
Clinical Research Staffing Reprioritizations and Resourcing Strategies
Gain insights on how to work through staffing reprioritizations and options to consider when planning resourcing strategies.
Industry-Wide Solutions to Improve Access to Clinical Trials
In this discussion, panelists provide actionable strategies for improving access to clinical research for diverse, underserved populations.
Budget Negotiation 101
Clinical trial costs vary from each site, and a prolonged budget negotiation process can affect the startup timeline.
Research Site Dramatically Increases Funding through Advarra’s Budget Negotiation Service
Utilizing Advarra’s Budget Negotiation Service enabled a research site to accelerate their timeline, alleviate budget negotiation burdens, and ensure their funding goals.
FDA Guidance on Shedding and Environmental Impact in Clinical Trials Involving Gene Therapy Products
Our IBC experts authored “FDA Guidance on Shedding and Environmental Impact in Clinical Trials Involving Gene Therapy Products” in Applied Biosafety.
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