Accelerating site activation can jumpstart a clinical trial, but with the hours and weeks spent manually tracking tasks and documents without visibility into where the bottlenecks lie, how can you make that happen?
Activate Cloud Service enables sponsors, CROs, and sites to get studies started in the shortest time possible. Activate workflows drive study teams to complete and track specific documents and tasks required for any site, country, or study based on regulatory and SOP requirements.
Drive superior study planning with study- and client-specific configurations in one application. Tight study startup management and cross departmental coordination ensure timely, accurate, and compliant submissions.
Reduce uncertainty in study execution with accurate predictive capabilities to auto-populate milestones, providing greater risk transparency and allowing informed data-driven decisions to be made.
Compare cycle time performance of studies against industry benchmarks for given study dimensions.
Leverage multi-plan comparison and visualization tools to help scenario plan optimal study setup to achieve enrollment goals in the fastest time possible.
The integration of industry proven study startup workflows with Cognizant's ® Shared Investigator Platform (SIP) accelerates clinical trials by standardizing administrative tasks and processes and bringing about increased efficiencies by minimizing redundant work.
Use visualizations and standardized metrics to aid in the identification of white space and machine learning algorithms to guide optimal timing of parallelization of processes to minimize risks associated with intervention.
Oracle Health Sciences end-to-end study startup solution stood out for the opportunity it provides us to eliminate traditional bottlenecks in the flow of clinical data, which can impact study quality and lead to unnecessary delays.
Learn the importance of this regulation and its impact on large multi-country studies.
Learn how decentralized clinical trials have forced the industry to rethink their approach to study startup and associated regulations.
Learn how the traditional steps needed to start clinical trials need to be expanded upon, collapsed, and fit for purpose.
The way clinical trials are conducted in the European Union will undergo a major change when this regulation comes into effect in January 2022, which is binding across all member states.
As CROs fight to maintain market share and ensure long-term survival, those capable of critical thinking and proactive planning may be well-positioned to reap the rewards.
Learn about forthcoming guidance which renews the focus on efficiencies in conducting clinical trials and provide tools to do so - significantly impacting oversight.
Learn how Pfizer successfully brought a highly effective and safe COVID-19 vaccine to market in under a year, and how these same breakthroughs could be applied to other studies.
Learn how trusted collaboration is key to keeping sponsor-CRO partnerships aligned on shared goals.
Learn how the focus on efficiency in ICH E6 (R3) will fundamentally change clinical trials.
Learn how machine learning can help identify and rectify systemic inefficiencies, allowing life science organizations to learn and adapt.
Learn how the collaboration between Cognizant and Oracle eliminates redundancy for sites and deliver better outcomes from sponsors/CROs.
Will the industry embrace this change or revert back to its old ways post-COVID-19?
Learn how vendor oversight can be implemented end-to-end, ensuring compliance with ICH regulation guidelines.
Learn how to gain critical operational insights by using AI/machine learning to transition from subjective decision making.
Learn how digital transformation roadmaps were accelerated to embrace innovative approaches to overcome adversary.
Clinical trials are constantly evolving, with advancements in technology, industry initiatives, and regulatory, and process changes. Gain perspective and learn more about these changes in the resources below.
Activate’s robust, industry proven library of country-specific workflows and management-based approach to site activation is central to our efforts to build out our infrastructure of ‘best of breed’ applications in our eClinical suite.