Accelerating Clinical Development
Anova accelerates and reduces the cost of clinical development through our services and technology. Our team of experts support the design and development of pre-clinical and clinical development programs, and analysis of data that result from them.
Using our OneSource™ technology platform, Anova reduces complexity in clinical development. We bring together all stakeholders in clinical research and use automation, innovative study design and continuous learning to increase the likelihood of marketing approval.
“You never change things by fighting the existing reality. To change something, build a new model that makes the existing model obsolete”
A Learning System
Anova’s OneSource™ technology provides a platform for science, informatics, incentives, and culture to align for continuous improvement and innovation, with best practices seamlessly embedded in the delivery process and new knowledge is captured as an integral by-product of the delivery experience.
We standardize and optimize clinical research operations to reduce cost and development time, and provide a platform to support open innovation and collaboration across the network.
OneSource™ synthesises clinical evidence captured across the clinical research enterprise for treatment decision support, clinical study design and studies of comparative effectiveness.
Anova’s technology platform, OneSource™, supports collaboration across all stakeholders in clinical research as part of a ‘learning system’ designed to address today’s broken system.
OneSource™ is a continuous learning environment the capture clinical evidence as part of an open innovation network that reuses that evidence to reduce the cost and time taken for clinical development.
Accelerated Clinical Research Operations
OneSource™ supports both design and conduct of both adaptive and traditionally phased studies. The solution provides:
• Network registration, essential document management and validation;
• Contracting and budgeting;
• Protocol design, clinical trial ID, research collaboration & education;
• Site ID, selection and just-in-time activation;
• IRB/IEC submission & approval;
• Core service provision;
• Just-in-time product & supplies management;
• Oversight & monitoring;
• Billing & payment;
• Master data management; and,
• Reporting & publication.
Clinical research reborn, less complex, more efficient.
NEWS, VIEWS, EVENTS AND SOCIAL FEEDS
For the latest news from Anova, join the conversation about how our network is changing clinical research as we know it, browse some of the favourites on our bookshelf, and find events where you can meet our team. View all news, views and events here.
Meet the Anova team at the Expanded Access Summit 2019 on the 22-23 January in Washington, DC. Hear from Anova CEO Christopher Beardmore who will present at the event a transformational new approach to Compassionate Use.read more
Over the past many months I have received news of the deaths of a 13 year old boy following his fight with glioblastoma multiforme, a software and technology innovator in Atlanta from urothelial cancer and a beloved high school teacher and close friend...read more
We don’t need new regulation to form n=1 trials and offer them to patients. It is time to stop looking for changes in regulation to give us permission to pursue these activities. In short it is time to deliver on the promise of precision medicine.read more
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