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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.
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.
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.
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.
Learn how fundamental to new ICH guidelines is the modernization of processes and technology with a focus on QbD and risk-based management approaches.
Learn how machine learning technologies can help predict outcomes in clinical trials, leading to faster drug approval times and lower costs.
Learn how to overcome the complexities introduced in outsourced studies (e.g., quality, oversight, collaboration, and governance).
Learn how entrenched silos have stymied data flow efforts due to minimal understanding of what is needed downstream.
Drive competitive performance and operational excellence by focusing on bottlenecks and processes ripe for optimization.
Learn how good clinical practice (GCP) guidelines and systems help improve overall study quality.
Learn how contemporariness can be defined in operational SOPs and implemented in daily operations to ensure audit readiness.
Learn how to tackle the challenge of improving budget and contract cycle times in starting clinical trials.
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.