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Clinical One

The only platform that truly unifies people, processes, and data to simplify and accelerate the clinical trials of today and in the future.

One platform, one build, one login, one place.

Clinical One Unified Platform

Maintain safety and quality

In the world of clinical research, speed—while maintaining quality and safety—is critical. But with multiple independent systems, operational effectiveness is a problem. The only way to markedly impact efficiency is to totally rethink the way technology supports the entire clinical trial lifecycle. With Oracle Health Sciences Clinical One Cloud Service (Clinical One), you can reimagine the way technology and information support clinical research. Clinical One is the only truly unified eClinical platform that harmonizes data, streamlines workflow, and saves significant time from study startup to study closeout.


Simplify data collection

With all the siloed systems used to conduct clinical trials today, it is no surprise that the scope and severity of data quality issues is an urgent problem. Clinical data is increasingly inconsistent, incompatible, incomplete, missing, or duplicated. In addition, these issues are exacerbated by the increasing volume and variety of new data now being collected in clinical trials. On top of this, visibility across functions and between sponsors and CROs remains a challenge—data issues can be missed, which can put regulatory approval at risk. With Clinical One, you can collect and manage all your data in one place. No more duplicate data entry, reconciliation, or hidden issues.


Remove redundancies

There is often a focus on isolated processes in clinical research, but to make a significant positive impact, you need to focus on workflow—the sequence of processes through which a clinical trial passes from initiation to completion. Taking this integrated view, you can see where the redundancies, bottlenecks, and slow-downs really are. In today’s multiple-point-solution eClinical environment, study teams manage numerous study builds, multiple validations, and complicated integration requirements, while sites struggle with a myriad of credentials, overwhelming training requirements, and a tsunami of daily email alerts from all of the systems they are required to use to participate in clinical research. With Clinical One, all these issues disappear. One platform, one build, one login, one place.


See why Oracle was named a leader in the 2020 Everest Group PEAK Matrix for eClinical.

How our customers experience Oracle for clinical research

Health Decisions achieves shorter clinical trial timelines with Oracle Clinical One
Servier selects Oracle's Clinical One to unify clinical operations

To support the needs of today’s clinical trials, and those of the future, you need a platform that is:

01 Unified

Single platform that supports all processes, people, workflow, data, and analytics.

02 Universal

Ingest any data source, format, frequency, and volume connected to any application target.

03 Open

Upstream and downstream integration with legacy systems and wider application ecosystem.

04 Flexible

Configure and scale for traditional, hybrid, or fully decentralized trials and support different patient choices.

Clinical trial adaptations made during the pandemic reveal an industry embracing change

Natalie Gagliordi, Senior Writer, Oracle

The methods utilized during the pandemic are likely to have a lasting impact on the future of clinical trials, according to a new research study conducted by Informa Pharma Intelligence and Oracle.

Read the complete post

Find resources and more

Top 5 Challenges of Decentralized Clinical Trials and How To Overcome Them

As COVID-19 began to spread around the world, life sciences organizations conducting clinical trials had to quickly adopt remote data collection technologies and processes to keep patients safe and clinical trials running.

Read the Clinical Leader article

Clinical Trial Management in a Post-Pandemic World

As we look toward a post-pandemic world, Oracle Health Sciences, in partnership with Informa Pharma Intelligence conducted a global, industry-wide survey to understand the adaptations that were made to clinical trials during the pandemic, the effect of these adaptations, and the impact of these changes on the future of clinical trials.

Read the report (PDF)

How to realize the efficiency benefits of ICH E6 (R3) before it’s released

ICH E6 (R3) is coming at a time when life science organizations are still struggling to adopt ICH E6 (R2). But should organizations wait until these guidelines are ratified to realize the intended benefits?

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