SITES
Podcast — Strategic Site Identification: A Proven Approach
Watch our new podcast to discover Altasciences' unique process for identifying and selecting the right clinical sites for your unique project.
Harnessing The Potential Of Patient-Level Data In Clinical Trials
Join our panel of industry leaders as they explore innovative methods and best practices for incorporating fully consented patient data in clinical trials.
What Does Site Engagement Actually Do?
Site Engagement stays close to research sites, providing guidance, reducing administrative strain, and addressing issues early. Their support keeps studies moving by preventing small operational challenges from becoming delays.
Designed To Help Sites Increase Clinical Trial Capacity
IQVIA One Home for Sites is a platform that serves as a neutral aggregator, connector, and communicator of the key systems and tasks a clinical research site needs to perform across all the trials it is conducting.
Elevating The Site-Sponsor Experience: SaaS-Based Feasibility And Site Selection For Clinical Trials
In this webinar, learn about the transformation clinical trial feasibility and site selection across the industry.
Effective Study Design And Execution Of Renal And Hepatic Impairment Trials
Master the complexities of renal and hepatic trials by leveraging site expertise and PK modeling to navigate recruitment challenges and ensure precise dosing for impaired populations.
Automatically Triggered Micropayments And Built-In Reporting
Automated micropayments and unified trial data ease site burdens, boost participant retention, and deliver real-time insights. Discover a better way to run clinical trials.
Scout's Honor | Patient Payments And Travel Made Easier
Clinical trials rely on smooth coordination between participants, sites, and sponsors. Payment, travel, and logistical support help reduce barriers, simplify administration, and keep studies moving forward.
Where The Data Starts: Rebuilding Sponsor-Site Alignment On Source
In this candid discussion, we cover the disconnect between sponsor-designed data systems and the way source data is actually created, managed, and verified at the site.
Tailored Sponsor Engagement Key To Unlocking Site Network Efficiency
Karri Venn, VP site advocacy and mentorship at SCRS, emphasized the importance of sponsors recognizing the structure and capabilities of larger site networks.
A Turnkey Solution For Clinical Trials In Australia
This presentation is centered on Australia's unique value proposition in the global research landscape, emphasizing its ability to deliver high-quality trials with speed and efficiency.
Should Sponsors Provide Source Document Templates?
Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.
Building One Home for Sites
Watch this presentation and demonstration of One Home for Sites for the latest updates on how the industry is coming together — even competitors — to alleviate the technology burden on research sites.
Trends In Sponsor-Of-Choice Initiatives: Consolidating Site Payments
Listen in as leaders from Bristol Myers Squibb, CenExel Centers of Excellence, and IQVIA Technologies discuss the importance of providing a consistent clinical trial payment experience to sites.
How To Drive Stronger Sponsor-Site Partnerships
Karri Venn of SCRS discussed the value of deep partnerships, referencing a Sanofi initiative (SMILE) that trusted sites with protocol input and offered maximum budgets without negotiation.
What Boosts Efficiency At Smaller Clinical Sites?
Devora Henderson, CEO of Elevate Clinical Research, highlighted the need for clear points of contact at smaller sites.
Adaptive Clinical Trials
An adaptive study design can be especially useful if there are uncertainties specific to your drug. Adjusting your study as data accumulates means getting answers sooner.
The Rise Of The Site: Empowering Efficient Clinical Study Execution
Join the Co-CEO of CRIO, as he explores research site challenges and how site-based technologies can reduce administrative burdens, enhance efficiency, and eliminate redundant one-time-use technologies.
Benefit From Enhanced Power And Intelligence
Find a supply automation value engine with intelligent automation and algorithms to analyze drug supply data and automatically adjust delivery quantities to each site based on data available in IRT.
Complex Trials, Clear Budgets: Global Clinical Trial Budgeting Strategies
Gain valuable insights into efficient budgeting strategies and discover how technology can offer a holistic solution for managing investigator grant costs.
Inside Look At Ophthalmic Early Clinical Research
Benefit from our integrated approach that combines clinical and scientific expertise specific to ophthalmology with our co-located Ophthalmic clinic.
How Merck Enhances Site Collaboration
Learn about Merck’s approach to fostering strong site relationships through specialty roles like institutional lead CRAs and site relationship managers.
Navigating Participant Payment Challenges: A New Approach For Sponsors And Sites
As trials grow more sophisticated and operate on a larger, global scale, understanding the nuances of participant payment management has become essential for sponsors and sites alike.
Korio RTSM Platform: Site User Experience
With minimal navigation, users of this platform can view a participant list, demographics, and status indicators — taking key actions like screening or randomizing without leaving the main grid.
Patient Payments And Travel
Eliminate financial and travel hurdles for trial participants. Unify payments and travel logistics to reduce site burden, boost participant retention, and run seamless studies.
Global Site Advocacy Group Meeting
Gain an understanding around site payment burdens and how our solutions can empower sites around the world.
Using Technology To Reduce Monitoring Costs And Increase Quality
Join industry experts as they discuss how the true value of DDC lies not just in the cost of the technology itself but in the operational efficiencies it unlocks.
Stay Audit-Ready: Practical Compliance Insights For Research Sites
Gain an auditors insight into common compliance gaps and learn practical ways to strengthen audit readiness in sIRB studies.
Multi-Site Capabilities For Your Phase I-II Trials
Master the complexities of renal and hepatic trials by leveraging site expertise and PK modeling to navigate recruitment challenges and ensure precise dosing for impaired patient populations.
Webinar: Reimbursement Methods For Sustainable CGT Business Models
Learn more about the key features of successful innovative pricing and reimbursement models as well as outcomes-based agreements and the ways to advance those strategies for cell and gene therapies.