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Clinical data, simply

CRScube is at the forefront of clinical data management.

Dedicated to empowering the pharmaceutical, biotechnology and medical device industries, we’re advancing technology and enhancing research efficiency. 

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Join us on a journey as we push the boundaries of what’s possible – and advance clinical trials together.

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studies delivered

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site users

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patients

Transforming your trials

Designed with your needs in mind, our unified suite of solutions simplifies your processes, helping accelerate research, improve data quality, and drive impactful results.

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Experience CRScube

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Supporting your medical breakthroughs

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Streamline trials, boost ROI

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Maximize value, minimize risks

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Enhance your competitive edge

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Clean, accurate data at your fingertips

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One platform, multiple solutions

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Affordable, scalable solutions

Empowering progress: our story

We are dedicated to developing impactful solutions that reshape trial management, enhance site operations, and improve patient experiences.

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Your clinical research ally

From study design to data analysis, we’ve got you covered thanks to end-to-end support.

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See CRScube in action

Explore how our platform will elevate your team and clinical trial management.

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Get insights straight to your inbox

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Explore our knowledge base

Stay in-the-know with regular updates and industry opinions from our expert team.

Featured resources

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7 essential questions to ask before choosing a safety reporting vendor

When selecting a pharmacovigilance solution, you need a system that not only ensures compliance but also enhances efficiency and scalability.

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Enhancing Pharmacovigilance with cubeSAFETY: A conversation with QVIS

We selected cubeSAFETY because of its robust compliance features, seamless integration with regulatory submission platforms, and its ability to handle large volumes of safety data efficiently.

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The promise and challenges of the Unified Study Definition Model (USDM)

Standardization that is industry-led is unlikely to be widely successful by itself, as there is no strong incentive to adhere to them. However, when it aligns with regulatory guidelines, the chance of a timely and successful implementation is increased.

Read more
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