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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.
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 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.
Discover how to combat poor risk management practices that have fueled the rescue study industry.
Hear how eClinical technologies and industry initiatives are impacting the ability of investigative sites to conduct clinical trials.
Learn how to mitigate the patient and data quality risks associated with decentralized 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.